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Audrone Urboniene 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 3010031584.

Audrone Urboniene

Kovno, -, Lithuania
Issue DateApril 26, 2013
FEI Number3010031584
CountryLithuania
Status
No Warning Letter
Product Type
Drugs
Audrone Urboniene FDA Form 483, Kovno, April 26, 2013