# The Biery Cheese Company, Louisville, OH – FDA Inspections

Source: https://www.keypedia.com/companies/the-biery-cheese-company/c2788485-35c2-48d5-813c-df2be15f4ba5

> Inspection records and compliance data for The Biery Cheese Company in Louisville, Ohio. 7 FDA inspections on record, 1 Form 483, last inspected November 29, 2023.

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## Details

- Name: The Biery Cheese Company
- FEI Number: 1520157
- Address Line 1: 6544 Paris Ave
- City: Louisville
- State: Ohio
- Zip Code: 44641
- Country Name: United States
- Address: 6544 Paris Ave, Louisville, Ohio 44641, United States
- Country: United States

## Related Documents

- [FDA Inspection 1225618 - The Biery Cheese Company - 2023-11-29](https://www.keypedia.com/records/fda_inspections/the-biery-cheese-company/0f97bca9-56c9-4434-a828-8cc5c1c5b0ad) — source: FDA, date: November 29, 2023
- FDA Inspection 1029046 - The Biery Cheese Company - 2017-09-18 — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2017
- [FDA Inspection 964566 - The Biery Cheese Company - 2016-03-18](https://www.keypedia.com/records/fda_inspections/the-biery-cheese-company/3c4ca8c7-2146-481a-871b-ce8b4fe2bc17) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2016
- FDA Inspection 809262 - The Biery Cheese Company - 2012-12-05 — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2012
- FDA Inspection 760881 - The Biery Cheese Company - 2011-12-29 — classification: No Action Indicated (NAI), source: FDA, date: December 29, 2011
- FDA Inspection 675703 - The Biery Cheese Company - 2010-08-09 — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2010
- FDA Inspection 675703 - The Biery Cheese Company - 2010-08-09 — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2010
- FDA Inspection 675703 - The Biery Cheese Company - 2010-08-09 — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2010
- FDA Inspection 572462 - The Biery Cheese Company - 2009-03-11 — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2009

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