FDA Warning Letter — Horiba Instruments Incorporated

Case 289898 — FEI 3002698356

The FDA took a Warning Letter action against Horiba Instruments Incorporated on July 25, 2012 (Irvine, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Horiba Instruments Incorporated
Date
July 25, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Irvine, CA (United States)