FDA Inspection 947607 — BioPro, Inc.

BioPro, Inc. — FEI 1832656

The FDA completed an inspection of BioPro, Inc. on October 7, 2015 in Port Huron, MI. 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
October 7, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Port Huron, MI (United States)