FDA Warning Letter — Bionetek Corporation

Case 166233 — FEI 3008740613

The FDA took a Warning Letter action against Bionetek Corporation on Apr 18, 2011 (El Monte, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Bionetek Corporation
Date
Apr 18, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
El Monte, CA (United States)