FDA Inspection 1288256 — GELITA AG
The FDA completed an inspection of GELITA AG on Jan 18, 2023 in Eberbach. 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)
- End Date
- Jan 18, 2023
- Fiscal Year
- 2023
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Eberbach (Germany)
Additional Details
Mutual Recognition Agreement (MRA)