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Eurofins Biopharma Product Testing Munich GmbH Form 483 Details

Form 483
Find this 483 on FDA
Source: FDA Data DashboardFDA has published this inspection and the number of observations cited. The form itself has not been released yet, which usually takes six to twelve months.
Check this firm on FDA, establishment 3003706029

Eurofins Biopharma Product Testing Munich GmbH

Planegg, -, Germany
Issue DateJuly 12, 2019
FEI Number3003706029
CountryGermany
Status
No Warning Letter
Product Type
Drugs
Eurofins Biopharma Product Testing Munich GmbH FDA Form 483, Planegg, July 12, 2019