FDA Inspection 1017591 — KREWE DU OPTIC
The FDA completed an inspection of KREWE DU OPTIC on Nov 1, 2016 in New Orleans, LA. 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
- Nov 1, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Orleans, LA (United States)