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Merck, Inc. Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 2210048.

Merck, Inc.

Kenilworth, New Jersey, United States
Issue DateSeptember 01, 2009
FEI Number2210048
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Merck, Inc. FDA Form 483, Kenilworth, New Jersey, September 1, 2009