FDA Inspection 934403 — Anika Therapeutics, Inc.
The FDA completed an inspection of Anika Therapeutics, Inc. on May 22, 2015 in Bedford, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- May 22, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bedford, MA (United States)