FDA Inspection 1056202 — Procedure Products, Inc.
The FDA completed an inspection of Procedure Products, Inc. on Jun 7, 2018 in Vancouver, WA. 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
- Jun 7, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vancouver, WA (United States)