FDA Inspection 1193899 — Aeropharm Gmbh
The FDA completed an inspection of Aeropharm Gmbh on June 6, 2022 in Rudolstadt. 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
- June 6, 2022
- Fiscal Year
- 2022
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Rudolstadt (Germany)
Additional Details
Mutual Recognition Agreement (MRA)