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FDA Inspection 934403 — Anika Therapeutics, Inc.

Anika Therapeutics, Inc. — FEI 3007093114

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 were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 22, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Bedford, MA (United States)

Facility

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FDA data resources