# Envoy Air - Inspection Records

Source: https://www.globalkeysolutions.net/companies/envoy-air/8fc6387f-a8ee-49ef-afa7-689f90d54279

> Inspection records and compliance data for Envoy Air in Cedar Rapids, Iowa. Access full analysis and detailed observations.

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## Details

- Name: Envoy Air
- FEI Number: 3007797898
- City: Cedar Rapids
- State: Iowa
- Country Name: United States
- Address Line 1: 2121 Arthur Collins Pkwy Sw
- Zip Code: 52404

## Related Documents

- [FDA Inspection 1215651 - Envoy Air - 2023-07-18](https://www.globalkeysolutions.net/records/fda_inspections/envoy-air/b721c6a6-2187-4d71-bb31-522670100613) — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2023
- [FDA Inspection 1215651 - Envoy Air - 2023-07-18](https://www.globalkeysolutions.net/records/fda_inspections/envoy-air/c105c481-261e-4ad0-a435-bc489d8d1178) — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2023
- [FDA Inspection 1070451 - Envoy Air - 2018-08-02](https://www.globalkeysolutions.net/records/fda_inspections/envoy-air/ff55ed9c-32b9-4871-b8ee-efb30ae5bd5b) — classification: No Action Indicated (NAI), source: FDA, date: August 2, 2018
- [FDA Inspection 947859 - Envoy Air - 2015-09-10](https://www.globalkeysolutions.net/records/fda_inspections/envoy-air/1c0efe74-bbf0-40ca-8391-ec6705692d19) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2015
- [FDA Inspection 837117 - Envoy Air - 2013-06-18](https://www.globalkeysolutions.net/records/fda_inspections/envoy-air/586c0957-cef7-4b8c-a24d-212b7532a060) — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2013
- [FDA Inspection 739724 - Envoy Air - 2011-06-29](https://www.globalkeysolutions.net/records/fda_inspections/envoy-air/8ad1d796-2b7b-4d27-9386-37d82baef423) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2011
- [FDA Inspection 607246 - Envoy Air - 2009-08-06](https://www.globalkeysolutions.net/records/fda_inspections/envoy-air/2e0dcc10-017a-4b49-bd1c-80109025ac34) — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2009

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