FDA Inspection 1089142 — Elanco UK AH Limited
The FDA completed an inspection of Elanco UK AH Limited on June 14, 2018 in Speke, Liverpool. 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 14, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Speke, Liverpool (United Kingdom)
Additional Details
Mutual Recognition Agreement (MRA)