# Remel, Inc - Inspection Records

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

> Inspection records and compliance data for Remel, Inc in Lenexa, Kansas. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1199839 - Remel, Inc - 2023-03-03](https://www.keypedia.com/records/fda_inspections/remel-inc/27f2b49e-c77a-48ba-b138-521f27b0ca72) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2023
- [FDA Inspection 1199839 - Remel, Inc - 2023-03-03](https://www.keypedia.com/records/fda_inspections/remel-inc/35ecfda3-b61c-4291-ba05-bf475ae22050) — 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](https://www.keypedia.com/records/fda_inspections/remel-inc/c3a29863-ae6f-4984-9fc6-db9099b24667) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 3, 2014
- [FDA Inspection 885210 - Remel, Inc - 2014-07-03](https://www.keypedia.com/records/fda_inspections/remel-inc/2b40499d-5ec8-4516-804d-ca7dbc55272e) — classification: No Action Indicated (NAI), source: FDA, date: July 3, 2014
- [FDA Inspection 836927 - Remel, Inc - 2013-06-25](https://www.keypedia.com/records/fda_inspections/remel-inc/8a7333ba-cf18-4d5f-8a5e-26d788846ba0) — 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](https://www.keypedia.com/records/fda_inspections/remel-inc/009c8ef8-abeb-4512-9d42-ff06f1f7eaba) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2013
- [FDA Inspection 658081 - Remel, Inc - 2010-03-18](https://www.keypedia.com/records/fda_inspections/remel-inc/9e14120c-c763-4da9-a8b0-22bd921f1b87) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2010
- [FDA Inspection 658081 - Remel, Inc - 2010-03-18](https://www.keypedia.com/records/fda_inspections/remel-inc/d480c567-509f-495b-be8b-dde4bc478581) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2010

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