FDA Inspection 1031306 — FABRITEQ LLC
The FDA completed an inspection of FABRITEQ LLC on Nov 1, 2017 in Knoxville, TN. 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
- Nov 1, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Knoxville, TN (United States)