FDA Inspection 1152158 — Tenex Health, Inc.

Tenex Health, Inc. — FEI 1000135560

The FDA completed an inspection of Tenex Health, Inc. on September 1, 2021 in Lake Forest, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 1, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Lake Forest, CA (United States)