FDA Inspection 1329620 — F. Hoffmann-La Roche AG

F. Hoffmann-La Roche AG — FEI 3002807200

The FDA completed an inspection of F. Hoffmann-La Roche AG on May 9, 2025 in Basel Town. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 9, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Basel Town (Switzerland)

Additional Details

Mutual Recognition Agreement (MRA)