FDA Inspection 1061626 — Bionica Inc.

Bionica Inc. — FEI 3004435660

The FDA completed an inspection of Bionica Inc. on July 16, 2018 in Mcclellan, CA. 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
July 16, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Mcclellan, CA (United States)