FDA Inspection 917365 — GP Pharm SA

GP Pharm SA — FEI 3008345811

The FDA completed an inspection of GP Pharm SA on January 27, 2015 in Sant Quinti De Mediona. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 27, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Quinti De Mediona (Spain)