FDA Inspection 802119 — Lonza Biologics Plc
The FDA completed an inspection of Lonza Biologics Plc on Sep 24, 2012 in Wokingham. 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
- Sep 24, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Wokingham (United Kingdom)