FDA Inspection 927998 — Promethean Surgical Devices, Inc.
The FDA completed an inspection of Promethean Surgical Devices, Inc. on May 8, 2015 in East Hartford, CT. 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
- May 8, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- East Hartford, CT (United States)