FDA Inspection 885452 — TIDI Products, LLC
The FDA completed an inspection of TIDI Products, LLC on Jun 25, 2014 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
- Jun 25, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Ontario, CA (United States)