FDA Warning Letter — Instratek, Incorporated

Case 347218 — FEI 1000118334

The FDA took a Warning Letter action against Instratek, Incorporated on August 23, 2012 (Houston, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Instratek, Incorporated
Date
August 23, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Houston, TX (United States)