FDA Inspection 848517 — HyperBranch Medical Technology, Inc.
The FDA completed an inspection of HyperBranch Medical Technology, Inc. on September 11, 2013 in Durham, NC. 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) (VAI)
- End Date
- September 11, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Durham, NC (United States)
Additional Details
Sponsor, Contract Research Organization