FDA Warning Letter — Tenex Health, Inc.

Case 47700 — FEI 1000135560

The FDA took a Warning Letter action against Tenex Health, Inc. on March 16, 2009 (Lake Forest, 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
Tenex Health, Inc.
Date
March 16, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Lake Forest, CA (United States)