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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
Bioresearch Monitoring
Location
Bedford, MA (United States)

Additional Details

Postmarket Audit Inspections

Facility

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FDA data resources