FDA Warning Letter — Tenex Health, Inc.

Case 313938 — FEI 1000135560

The FDA took a Warning Letter action against Tenex Health, Inc. on June 14, 2012 (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
June 14, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Lake Forest, CA (United States)