FDA Inspection 766406 — Bausch & Lomb, Inc.
The FDA completed an inspection of Bausch & Lomb, Inc. on Jan 19, 2012 in Manchester, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 19, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Manchester, MO (United States)