# Christian Cheese, LLC, Kingfisher, OK – FDA Inspections

Source: https://www.keypedia.com/companies/christian-cheese-llc/cfdcc1f3-3f36-4fd5-ba1a-d74db0e29f01

> Inspection records and compliance data for Christian Cheese, LLC in Kingfisher, Oklahoma. 6 FDA inspections on record, last inspected July 11, 2022.

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## Details

- Name: Christian Cheese, LLC
- FEI Number: 3003077811
- Address Line 1: 13 Airport Road
- City: Kingfisher
- State: Oklahoma
- Zip Code: 73750
- Country Name: United States
- Address: 13 Airport Road, Kingfisher, Oklahoma 73750, United States
- Country: United States

## Related Documents

- FDA Inspection 1174126 - Christian Cheese, LLC - 2022-07-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 11, 2022
- [FDA Inspection 1174126 - Christian Cheese, LLC - 2022-07-11](https://www.keypedia.com/records/fda_inspections/christian-cheese-llc/6ac72a6b-db6b-4c59-b2df-059369e2c49e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 11, 2022
- FDA Inspection 1065496 - Christian Cheese, LLC - 2018-07-02 — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2018
- [FDA Inspection 933836 - Christian Cheese, LLC - 2015-07-02](https://www.keypedia.com/records/fda_inspections/christian-cheese-llc/2d988dd8-5017-4c88-a5c8-863ae6903a2b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2015
- FDA Inspection 833237 - Christian Cheese, LLC - 2013-04-29 — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2013
- FDA Inspection 790579 - Christian Cheese, LLC - 2012-06-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2012
- FDA Inspection 740648 - Christian Cheese, LLC - 2011-08-19 — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2011
- FDA Inspection 740648 - Christian Cheese, LLC - 2011-08-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 19, 2011
- FDA Inspection 740648 - Christian Cheese, LLC - 2011-08-19 — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2011

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