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Nordmark Pharma GmbH 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 3003293533.

Nordmark Pharma GmbH

Uetersen, -, Germany
Issue DateNovember 20, 2014
FEI Number3003293533
CountryGermany
Status
No Warning Letter
Product Type
Drugs
Nordmark Pharma GmbH FDA Form 483, Uetersen, November 20, 2014