FDA Inspection 1066010 — Tenacore LLC

Tenacore LLC — FEI 3008403701

The FDA completed an inspection of Tenacore LLC on Aug 22, 2018 in Costa Mesa, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 22, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Costa Mesa, CA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation