FDA Inspection 1305638 — allphamed PHARBIL Arzneimittel GmbH

allphamed PHARBIL Arzneimittel GmbH — FEI 3008587095

The FDA completed an inspection of allphamed PHARBIL Arzneimittel GmbH on November 19, 2024 in Gottingen. 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
November 19, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gottingen (Germany)

Additional Details

Mutual Recognition Agreement (MRA)