FDA Inspection 885905 — Bioplate Inc

Bioplate Inc — FEI 1000518793

The FDA completed an inspection of Bioplate Inc on July 2, 2014 in Placentia, 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 2, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Placentia, CA (United States)