FDA Inspection 1124019 — Abbvie Ireland NL B.V.
The FDA completed an inspection of Abbvie Ireland NL B.V. on Feb 28, 2020 in Sligo. 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
- Feb 28, 2020
- Fiscal Year
- 2020
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Sligo (Ireland)
Additional Details
Mutual Recognition Agreement (MRA)