FDA Inspection 1123541 — Mylan Teoranta
The FDA completed an inspection of Mylan Teoranta on Jun 22, 2018 in Inverin. 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
- Jun 22, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Inverin (Ireland)
Additional Details
Mutual Recognition Agreement (MRA)