# MN Airlines LLC (dba) Sun Country Airlines, San Diego, CA – FDA Inspections

Source: https://www.keypedia.com/companies/mn-airlines-llc-dba-sun-country-airlines/5d31fec5-ef48-4d56-9376-9d9cfaca006a

> Inspection records and compliance data for MN Airlines LLC (dba) Sun Country Airlines in San Diego, California. 5 FDA inspections on record (1 OAI), 1 warning letter, last inspected February 06, 2017.

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## Details

- Name: MN Airlines LLC (dba) Sun Country Airlines
- FEI Number: 3007725061
- Address Line 1: 3707 N Harbor Dr Ste 126
- City: San Diego
- State: California
- Zip Code: 92101
- Country Name: United States
- Address: 3707 N Harbor Dr Ste 126, San Diego, California 92101, United States
- Country: United States

## Related Documents

- FDA Inspection 1004942 - MN Airlines LLC (dba) Sun Country Airlines - 2017-02-06 — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2017
- [FDA Inspection 898154 - MN Airlines LLC (dba) Sun Country Airlines - 2014-09-29](https://www.keypedia.com/records/fda_inspections/mn-airlines-llc-dba-sun-country-airlines/a92768f2-70c8-445c-9dff-1d5dc9aac3c4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 29, 2014
- FDA Inspection 846114 - MN Airlines LLC (dba) Sun Country Airlines - 2013-08-28 — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2013
- FDA Inspection 734464 - MN Airlines LLC (dba) Sun Country Airlines - 2011-07-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 13, 2011
- [WARNING_LETTER - MN Airlines LLC (dba) Sun Country Airlines - 2010-06-21](https://www.keypedia.com/records/warning_letter/mn-airlines-llc-dba-sun-country-airlines/49befd9e-a7c7-485f-9dc4-eef689d89736) — source: FDA, date: June 21, 2010
- [FDA Inspection 667747 - MN Airlines LLC (dba) Sun Country Airlines - 2010-06-21](https://www.keypedia.com/records/fda_inspections/mn-airlines-llc-dba-sun-country-airlines/20732d78-96ad-4da4-a7e8-6a6fad03e3d7) — classification: Official Action Indicated (OAI), source: FDA, date: June 21, 2010

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