FDA Inspection 1161536 — TIDI Products, LLC

TIDI Products, LLC — FEI 3016004577

The FDA completed an inspection of TIDI Products, LLC on Dec 9, 2021 in Ontario, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 9, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ontario, CA (United States)