FDA Inspection 762651 — Biogenex Laboratories, Inc.

Biogenex Laboratories, Inc. — FEI 2936532

The FDA completed an inspection of Biogenex Laboratories, Inc. on Jan 26, 2012 in Fremont, 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 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Fremont, CA (United States)

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