FDA Inspection 743472 — Bioplate Inc

Bioplate Inc — FEI 1000518793

The FDA completed an inspection of Bioplate Inc on September 1, 2011 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
September 1, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Placentia, CA (United States)