Question about NEC ETJ 16DD-2 Corded Phone

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On the LCD show code FDA 112 whats the meaning of ?

On display show Fda 112 in etj 16dd when I call from other extension. What I supposed to do.

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  • theo835 Apr 14, 2009

    I already try by press number 42 after press speaker but it doesn't work. Any other way ?

  • theo835 Apr 15, 2009

    I call from the other extension e.g 111 to the etj 16dd as hunting number. I mention hunting number why ? Coz if there are incoming calls the etj 16dd the operator will delivery to other extension. So I make conclusion that etj 16dd is PBX system. Can you help me ?

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  • 63 Answers

From the phone that is forwarde hit speaker key dial 42 should be cancel code for forwarding

Posted on Apr 13, 2009

  • victor8191 Apr 14, 2009

    what type of system is your phone system.A NEC KEY SYSTEM OR IS IT A PBX SYSTEM?

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1 Answer

What is this nutrio2


It is a supplement. The FDA does not perform studies as to the effectiveness of supplements. Rather, the FDA merely measures the purity of the ingredients. No supplement will even say the FDA supports claims as to the effects of a supplement. Often, the question as to just how much of a substance is actually in a pill is not clear. A pill can be an amalgamation of ingredients. So, even if you encounter science supporting effectiveness of an individual ingredient, the pill you encounter may have an insufficient amount to produce the same effect as in the study. Studies are supposed to be replicable. Just the fact that one study supports a contention is not an indicator that the study has been replicated elsewhee with the same results. I do not go into what nutrio2 is simply because I have no idea of what science supports any claims. I am sure you can look up the claims.

May 23, 2017 | Miscellaneous

2 Answers

Is DoTerra FDA approved or is that false?


It is False, they do not have FDA approval . Actually, please see linked letter below from FDA to DoTerra about their "claims" and what their ingredients actually are for. FDA says only use DoTerra if prescribed by a doctor.

I've pulled the most important part out:
"Your products are prescription drugs as defined in section 503(b)(1)(A) of the Act [21 U.S.C. § 353(b)(1)(A)]) for some of the claims made for them because, in light of their toxicity or other potentiality for harmful effect, the method of their use, or the collateral measures necessary to their use, they are not safe for use except under the supervision of a practitioner licensed by law to administer them."

dTERRA International LLC 9 22 14

Dec 01, 2014 | DoTerra Essential Oils For Healing

1 Answer

Is doTerra fda approved


Nope. Actually, please see linked letter below from FDA to DoTerra about their "claims" and what their ingredients actually are for.

dTERRA International LLC 9 22 14

Dec 01, 2014 | Health & Beauty

1 Answer

Does the FDA check dietary supplements before they are sold?


The FDA does not check dietary supplements. It is up to the supplement's manufacturer to make sure their product is safe and that the list of ingredients on the label matches the ingredients found in the product.

According to the FDA's website: "Generally, manufacturers do not need to register their products with FDA nor get FDA approval before producing or selling dietary supplements.* Manufacturers must make sure that product label information is truthful and not misleading. Under the FDA Final Rule 21 CFR 111, all domestic and foreign companies that manufacture, package, label or hold dietary supplement, including those involved with testing, quality control, and dietary supplement distribution in the U.S., must comply with the Dietary Supplement Current Good Manufacturing Practices (cGMPS) for quality control."

Also, if you notice, supplements always contain the following sentence below the nutrition facts and other information after the nutrition facts: "These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease."

Feb 04, 2013 | Health & Beauty

1 Answer

Who tests the content of the supplements?


The supplement companies are required to test their own products and make sure that the supplement facts and ingredient list are correct. The FDA does not evaluate supplements and it is under the sole responsibility of the supplement companies to make sure that their supplements are safe.

Feb 04, 2013 | Health & Beauty

1 Answer

Does maybelline use lead in their product???


Maybelline is owned by L'Oreal.And yes they do use lead . Cosmetics are not subject to pre-market approval by FDA. However, pre-market approval is required for the color additives used in cosmetics (including those in lipsticks) and other FDA-regulated products (with the exception of coal-tar hair dyes). To learn more on this subject, please refer to FDA Authority Over Cosmetics1.

Jun 13, 2011 | Maybelline Great Wear Waterproof Eyeliner...

1 Answer

What actions can the FDA take against manufacturers that produce and market unsafe cosmetics?


Consumer safety is the number one priority for cosmetic and personal care products companies, and manufacturers are committed to upholding strict FDA regulations as required by the U.S. Food, Drug, and Cosmetic Act (FD&C Act). The law requires that every cosmetic and personal care product and its ingredients be substantiated for safety before going to market, and that they contain no prohibited ingredients. Cosmetic companies take their safety responsibility very seriously and often surpass the requirements of the law with additional consumer safety measures.

Consumers must have confidence in the products they buy and use each day. Toward that end, cosmetic and personal care products companies invest substantial resources in scientific research and safety processes to ensure the safety of their products. Companies work with and employ thousands of chemists, toxicologists, biologists, environmental scientists and other experts to evaluate the safety of cosmetic products before they go to market.

As a result, of the more than 11 billion personal care products sold each year in the United States, there are very few adverse experiences reported to the FDA in a typical year, and of those reported, most are related to rashes or allergies. Cosmetic companies' strong commitment to safety has made cosmetic and personal care products the safest product category regulated by the FDA.

Nov 22, 2010 | Health & Beauty

2 Answers

Doesn’t the government certify that personal care products are safe and healthy before they can be sold to consumers?


No. Major loopholes in federal law allow the $50 billion cosmetics industry to put unlimited amounts of chemicals into personal care products with no required testing, no required monitoring of health effects, and inadequate labeling requirements.

Neither cosmetic products nor cosmetic ingredients are reviewed or approved by the Food and Drug Administration (FDA) before they are sold to the public. FDA cannot require companies to do safety testing of their cosmetic products before marketing

Nov 22, 2010 | Health & Beauty

4 Answers

FDA Lock


I have never heard of FDA lock. If you mean FPA lock, this is the Front Panel Access lock (also called Child Lock) built into the TV. To unlock FPA, turn the set on with the original remote, enter the menu, navigate to the page with FPA and set it to off.

Aug 21, 2007 | RCA 20F420T 20" TV

1 Answer

Mic


If the MIC lite is not lit you must press "FNC 1" to activate the microphone. If the MIC lite is lit but the problem persists, the extension is not programmed to be handsfree or you may possibly have a bad phone. If the extension needs to be programmed handsfree, it will need to be done by a qualified tech.

Apr 28, 2007 | NEC ETJ 16DD-2 Corded Phone

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