FDA Inspection 1112820 — McDermott Laboratories Ltd. Trading As Mylan Dublin Respiratory
The FDA completed an inspection of McDermott Laboratories Ltd. Trading As Mylan Dublin Respiratory on Jan 19, 2019 in Dublin. 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
- Jan 19, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Dublin (Ireland)
Additional Details
Mutual Recognition Agreement (MRA)