FDA Inspection 948191 — Product Quest Manufacturing LLC
The FDA completed an inspection of Product Quest Manufacturing LLC on Nov 6, 2015 in Daytona Beach, FL. 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
- Nov 6, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Daytona Beach, FL (United States)