FDA Inspection 1128748 — GBA Pharma GmbH

GBA Pharma GmbH — FEI 3004969119

The FDA completed an inspection of GBA Pharma GmbH on July 9, 2020 in Ulm. 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
July 9, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ulm (Germany)

Additional Details

Mutual Recognition Agreement (MRA)