# KORR Medical Technologies, Inc., Salt Lake City, UT – FDA Inspections

Source: https://www.keypedia.com/companies/korr-medical-technologies-inc/0ff5c8a9-9b3e-4bcc-b8b8-97e4e6b2e80d

> Inspection records and compliance data for KORR Medical Technologies, Inc. in Salt Lake City, Utah. 4 FDA inspections on record, 1 Form 483, last inspected March 17, 2022.

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## Details

- Name: KORR Medical Technologies, Inc.
- FEI Number: 3002892786
- Address Line 1: 3487 W 2100 S Ste 300
- City: Salt Lake City
- State: Utah
- Zip Code: 84119
- Country Name: United States
- Address: 3487 W 2100 S Ste 300, Salt Lake City, Utah 84119, United States
- Country: United States

## Related Documents

- [483 - KORR Medical Technologies, Inc. - 2022-03-17](https://www.keypedia.com/records/483/korr-medical-technologies-inc/c7ad9468-9369-4442-bada-e409134b60f0) — source: FDA, date: March 17, 2022
- FDA Inspection 1164820 - KORR Medical Technologies, Inc. - 2022-03-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 17, 2022
- FDA Inspection 1164820 - KORR Medical Technologies, Inc. - 2022-03-17 — classification: No Action Indicated (NAI), source: FDA, date: March 17, 2022
- [FDA Inspection 991323 - KORR Medical Technologies, Inc. - 2016-11-07](https://www.keypedia.com/records/fda_inspections/korr-medical-technologies-inc/2cb49d36-690a-4b7a-ac73-e651530e1418) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 7, 2016
- FDA Inspection 878261 - KORR Medical Technologies, Inc. - 2014-05-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2014
- FDA Inspection 878261 - KORR Medical Technologies, Inc. - 2014-05-10 — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2014
- FDA Inspection 722658 - KORR Medical Technologies, Inc. - 2011-05-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 3, 2011
- FDA Inspection 722658 - KORR Medical Technologies, Inc. - 2011-05-03 — classification: No Action Indicated (NAI), source: FDA, date: May 3, 2011

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