# Remel, Inc, Lenexa, KS – FDA Inspections

Source: https://www.keypedia.com/companies/remel-inc/f75612ef-610e-4ee4-980b-47569a492300

> Inspection records and compliance data for Remel, Inc in Lenexa, Kansas. 7 FDA inspections on record, last inspected March 03, 2023.

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## Details

- Name: Remel, Inc
- FEI Number: 1924669
- Address Line 1: 12076 Santa Fe Trail Dr
- City: Lenexa
- State: Kansas
- Zip Code: 66215
- Country Name: United States
- Address: 12076 Santa Fe Trail Dr, Lenexa, Kansas 66215, United States
- Country: United States

## Related Documents

- FDA Inspection 1199839 - Remel, Inc - 2023-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2023
- FDA Inspection 1199839 - Remel, Inc - 2023-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2023
- [FDA Inspection 953769 - Remel, Inc - 2015-10-23](https://www.keypedia.com/records/fda_inspections/remel-inc/cbd34b65-40d7-4b42-ba0b-9de05b2f11af) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 23, 2015
- FDA Inspection 885210 - Remel, Inc - 2014-07-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 3, 2014
- FDA Inspection 885210 - Remel, Inc - 2014-07-03 — classification: No Action Indicated (NAI), source: FDA, date: July 3, 2014
- FDA Inspection 836927 - Remel, Inc - 2013-06-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 25, 2013
- [FDA Inspection 836927 - Remel, Inc - 2013-06-25](https://www.keypedia.com/records/fda_inspections/remel-inc/c54b0fbe-4d6d-492d-8bba-515eb1f484a8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 25, 2013
- FDA Inspection 823206 - Remel, Inc - 2013-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2013
- FDA Inspection 658081 - Remel, Inc - 2010-03-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2010
- FDA Inspection 658081 - Remel, Inc - 2010-03-18 — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2010

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