FDA Inspection 1164820 — KORR Medical Technologies, Inc.

KORR Medical Technologies, Inc. — FEI 3002892786

The FDA completed an inspection of KORR Medical Technologies, Inc. on Mar 17, 2022 in Salt Lake City, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 17, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Salt Lake City, UT (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
316821 CFR 820.198(a)Complaints
333121 CFR 820.181DMR - not or inadequately maintained
341521 CFR 820.22Quality Audit/Reaudit - conducted
369621 CFR 820.100(b)Documentation