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Recipharm Uppsala AB 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 1000171246.

Recipharm Uppsala AB

Uppsala, -, Sweden
Issue DateMarch 14, 2014
FEI Number1000171246
CountrySweden
Status
No Warning Letter
Product Type
Drugs
Recipharm Uppsala AB FDA Form 483, Uppsala, March 14, 2014