FDA Inspection 978030 — Bausch & Lomb Inc
The FDA completed an inspection of Bausch & Lomb Inc on Jun 10, 2016 in Saint Louis, 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
- Jun 10, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Saint Louis, MO (United States)