FDA Inspection 826508 — Lonza AG
The FDA completed an inspection of Lonza AG on April 12, 2013 in Visp. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- April 12, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Visp (Switzerland)