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