FDA Inspection 556024 — ALLERGAN
The FDA completed an inspection of ALLERGAN on November 20, 2008 in Heredia. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 20, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Heredia (Costa Rica)
Additional Details
Postmarket Audit Inspections