FDA Inspection 763361 — St Louis Ophthalmic Equip
The FDA completed an inspection of St Louis Ophthalmic Equip on Jan 17, 2012 in Olivette, 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 17, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Olivette, MO (United States)