# Wrege Fish Company, Saginaw, MI – FDA Inspections

Source: https://www.keypedia.com/companies/wrege-fish-company/26036601-4513-4e4c-9505-e377612a4110

> Inspection records and compliance data for Wrege Fish Company in Saginaw, Michigan. 7 FDA inspections on record, 2 Form 483s, last inspected November 29, 2023.

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## Details

- Name: Wrege Fish Company
- FEI Number: 1000220726
- Address Line 1: 226 Millard St
- City: Saginaw
- State: Michigan
- Zip Code: 48607
- Country Name: United States
- Address: 226 Millard St, Saginaw, Michigan 48607, United States
- Country: United States

## Related Documents

- [FDA Inspection 1225279 - Wrege Fish Company - 2023-11-29](https://www.keypedia.com/records/fda_inspections/wrege-fish-company/666ca8d3-a6fe-4d46-9f28-05c83e6c8258) — source: FDA, date: November 29, 2023
- [FDA Inspection 1056946 - Wrege Fish Company - 2018-06-26](https://www.keypedia.com/records/fda_inspections/wrege-fish-company/6a8d6cc9-2922-4d95-9762-44569537b27e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 26, 2018
- [FDA Inspection 931232 - Wrege Fish Company - 2015-06-29](https://www.keypedia.com/records/fda_inspections/wrege-fish-company/d0945343-00e1-4873-8f99-eccf6746d27a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2015
- FDA Inspection 895044 - Wrege Fish Company - 2014-09-10 — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2014
- [FDA Inspection 808230 - Wrege Fish Company - 2012-11-26](https://www.keypedia.com/records/fda_inspections/wrege-fish-company/89931edb-ad5f-46a5-8676-e6749b29ac51) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 26, 2012
- FDA Inspection 707129 - Wrege Fish Company - 2010-12-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 30, 2010
- [FDA Inspection 655835 - Wrege Fish Company - 2010-04-05](https://www.keypedia.com/records/fda_inspections/wrege-fish-company/348c4a1e-b7be-4361-a24c-8518c287f603) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 5, 2010

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