FDA Inspection 909310 — C&E GP Specialists Inc.
The FDA completed an inspection of C&E GP Specialists Inc. on Aug 6, 2014 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 6, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- San Diego, CA (United States)