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