FDA Inspection 1097017 — Lonza Biologics Plc
The FDA completed an inspection of Lonza Biologics Plc on Sep 5, 2018 in Slough. 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)
- End Date
- Sep 5, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Slough (United Kingdom)
Additional Details
Mutual Recognition Agreement (MRA)