FDA Inspection 868807 — Anika Therapeutics S.r.l
The FDA completed an inspection of Anika Therapeutics S.r.l on February 10, 2014 in Padova. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 10, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Padova (Italy)