# Stone Bridge Cheese Company - Inspection Records

Source: https://www.keypedia.com/companies/stone-bridge-cheese-company/c7480a5d-313b-4901-bc43-4d4ed33dc51d

> Inspection records and compliance data for Stone Bridge Cheese Company in Waldo, Maine. Access full analysis and detailed observations.

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## Details

- Name: Stone Bridge Cheese Company
- FEI Number: 1293111
- City: Waldo
- State: Maine
- Country Name: United States
- Address Line 1: 75 Birches Rd
- Zip Code: 04915

## Related Documents

- [FDA Inspection 1197491 - Stone Bridge Cheese Company - 2023-01-24](https://www.keypedia.com/records/fda_inspections/stone-bridge-cheese-company/af83bd61-2709-4cfe-b99a-823e23a7c27e) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2023
- [FDA Inspection 1030595 - Stone Bridge Cheese Company - 2017-11-03](https://www.keypedia.com/records/fda_inspections/stone-bridge-cheese-company/484996e2-b651-47b2-a1db-88b70eab9a8f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2017
- [FDA Inspection 945441 - Stone Bridge Cheese Company - 2015-07-21](https://www.keypedia.com/records/fda_inspections/stone-bridge-cheese-company/b32996a6-8374-4662-9c14-637f93fb34b8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2015
- [FDA Inspection 787514 - Stone Bridge Cheese Company - 2012-06-21](https://www.keypedia.com/records/fda_inspections/stone-bridge-cheese-company/b1809769-50c1-4e61-89c8-86fc7c7201d4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 21, 2012
- [FDA Inspection 787514 - Stone Bridge Cheese Company - 2012-06-21](https://www.keypedia.com/records/fda_inspections/stone-bridge-cheese-company/4ba4eae2-d231-4a30-9020-e2a35929f7bc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 21, 2012
- [FDA Inspection 614586 - Stone Bridge Cheese Company - 2009-09-23](https://www.keypedia.com/records/fda_inspections/stone-bridge-cheese-company/09a2b93f-aab9-4cf2-93aa-7e0e18948bb8) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2009

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