FDA Inspection 679641 — Procedure Products, Inc.
The FDA completed an inspection of Procedure Products, Inc. on Aug 25, 2010 in Vancouver, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 25, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vancouver, WA (United States)