FDA Inspection 1117521 — Regeneron Ireland Designated Activity Company
The FDA completed an inspection of Regeneron Ireland Designated Activity Company on September 27, 2019 in Limerick. 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
- September 27, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Limerick (Ireland)
Additional Details
Mutual Recognition Agreement (MRA)