# Ruleau Bros, Inc. DBA Door County Whitefish, Stephenson, MI – FDA Inspections

Source: https://www.keypedia.com/companies/ruleau-bros-inc-dba-door-county-whitefish/834423da-97af-4b79-93f1-fc198bfeac76

> Inspection records and compliance data for Ruleau Bros, Inc. DBA Door County Whitefish in Stephenson, Michigan. 6 FDA inspections on record, 2 Form 483s, last inspected January 29, 2024.

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## Details

- Name: Ruleau Bros, Inc. DBA Door County Whitefish
- FEI Number: 1823362
- Address Line 1: W 521 South Drive
- City: Stephenson
- State: Michigan
- Zip Code: 49887
- Country Name: United States
- Address: W 521 South Drive, Stephenson, Michigan 49887, United States
- Country: United States

## Related Documents

- FDA Inspection 1230046 - Ruleau Bros, Inc. DBA Door County Whitefish - 2024-01-29 — source: FDA, date: January 29, 2024
- [FDA Inspection 1099041 - Ruleau Bros, Inc. DBA Door County Whitefish - 2019-07-30](https://www.keypedia.com/records/fda_inspections/ruleau-bros-inc-dba-door-county-whitefish/a6bddf1f-86ae-4fc8-bcdc-f015b05948d0) — source: FDA, date: July 30, 2019
- [FDA Inspection 1027550 - Ruleau Bros, Inc. DBA Door County Whitefish - 2017-09-07](https://www.keypedia.com/records/fda_inspections/ruleau-bros-inc-dba-door-county-whitefish/1aefa4f3-2305-40e6-ac86-834c3f92f733) — source: FDA, date: September 7, 2017
- [FDA Inspection 844239 - Ruleau Bros, Inc. DBA Door County Whitefish - 2013-08-14](https://www.keypedia.com/records/fda_inspections/ruleau-bros-inc-dba-door-county-whitefish/33bc37f4-e62b-49c9-a336-5c0b6f1ead6f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 14, 2013
- [FDA Inspection 729932 - Ruleau Bros, Inc. DBA Door County Whitefish - 2011-06-15](https://www.keypedia.com/records/fda_inspections/ruleau-bros-inc-dba-door-county-whitefish/23ed5496-8e2c-4a1c-ac4e-358d422531d4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2011
- FDA Inspection 674004 - Ruleau Bros, Inc. DBA Door County Whitefish - 2010-07-28 — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2010

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