FDA Inspection 1059152 — Blanchard Contact Lens, Inc.
The FDA completed an inspection of Blanchard Contact Lens, Inc. on Jul 9, 2018 in Manchester, NH. 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
- Jul 9, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Manchester, NH (United States)