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An FDA warning letter is an official message from the United States Food and Drug Administration (FDA) to a manufacturer or other organization that has violated some rule in a federally regulated activity. ... a correspondence that notifies regulated industry about violations that FDA has documented during its inspections or investigations.
The purpose of this WikiProject is to standardise and improve user warning templates, and make them conform to technical guidelines. User talk templates are placed on users' talk pages to advise a user against actions that disrupt Wikipedia, to advise editors of common mistakes, or to place a standard boilerplate note at the top of a page.
For welcome templates, see Category:Welcome templates. This category includes all of the user warning templates. Some of these templates are used by a large number of editors and admins involved in user disputes, so changes to them should be made with care. In general, these templates should be placed on a user's talk page.
To use a user warning template, choose a standardised template from the main page of the WikiProject on User Warnings. Every template has a family of about four levels, from a polite pointer to the sandbox to a stern demand that they desist or face consequences. It's not necessary to start at the first level; rather, you should choose one based ...
April 25, 2024 at 12:13 PM. (Reuters) -The U.S. health regulator has sent a warning letter to Cardinal Health after an inspection of its facility in Illinois found the company was marketing and ...
Generally includes "Please stop" or "Stop". Level 4 – Final warning – Assumes bad faith, strong cease and desist, last warning. Level 4im – Only warning – Assumes bad faith, very strong cease and desist, first and only warning. Generally used in the case of excessive or continuous disruption from a user or specific IP.