FDA Inspection 669781 — Brevet, Inc.

Brevet, Inc. — FEI 2025870

The FDA completed an inspection of Brevet, Inc. on June 30, 2010 in Irvine, 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
June 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)