FDA Inspection 655775 — Anika Therapeutics, Inc.
The FDA completed an inspection of Anika Therapeutics, Inc. on Mar 12, 2010 in Bedford, MA. 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
- Mar 12, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Bedford, MA (United States)
Additional details
Sponsor, Contract Research Organization