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Argen Corporation, The 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 2433919.

Argen Corporation, The

San Diego, California, United States
Issue DateDecember 12, 2013
FEI Number2433919
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Argen Corporation, The FDA Form 483, San Diego, California, December 12, 2013