FDA Inspection 1305252 — GP Pharm SA

GP Pharm SA — FEI 3008345811

The FDA completed an inspection of GP Pharm SA on September 21, 2023 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
September 21, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Quinti De Mediona (Spain)

Additional Details

Mutual Recognition Agreement (MRA)