FDA Inspection 641484 — Ormco Corporation

Ormco Corporation — FEI 2024258

The FDA completed an inspection of Ormco Corporation on Jan 14, 2010 in Pomona, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 14, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Pomona, CA (United States)