# Barry Farm Enterprises, Wapakoneta, OH – FDA Inspections

Source: https://www.keypedia.com/companies/barry-farm-enterprises/07b83677-b6f7-41b9-810a-c716b5ee5531

> Inspection records and compliance data for Barry Farm Enterprises in Wapakoneta, Ohio. 5 FDA inspections on record, last inspected May 21, 2019.

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## Details

- Name: Barry Farm Enterprises
- FEI Number: 3003147762
- Address Line 1: 20086 Mudsock Rd
- City: Wapakoneta
- State: Ohio
- Zip Code: 45895
- Country Name: United States
- Address: 20086 Mudsock Rd, Wapakoneta, Ohio 45895, United States
- Country: United States

## Related Documents

- FDA Inspection 1092957 - Barry Farm Enterprises - 2019-05-21 — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2019
- FDA Inspection 730530 - Barry Farm Enterprises - 2011-05-18 — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2011
- FDA Inspection 730530 - Barry Farm Enterprises - 2011-05-18 — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2011
- FDA Inspection 730530 - Barry Farm Enterprises - 2011-05-18 — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2011
- FDA Inspection 725143 - Barry Farm Enterprises - 2011-05-18 — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2011
- [FDA Inspection 725143 - Barry Farm Enterprises - 2011-05-18](https://www.keypedia.com/records/fda_inspections/barry-farm-enterprises/cc495fd1-d052-4944-8a3b-ea6d4a04e114) — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2011
- FDA Inspection 725143 - Barry Farm Enterprises - 2011-05-18 — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2011
- FDA Inspection 609889 - Barry Farm Enterprises - 2009-09-03 — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2009
- FDA Inspection 609889 - Barry Farm Enterprises - 2009-09-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 3, 2009
- FDA Inspection 609889 - Barry Farm Enterprises - 2009-09-03 — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2009

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