# Hirzel Canning Company, Pemberville, OH – FDA Inspections

Source: https://www.keypedia.com/companies/hirzel-canning-company/7e332682-e392-4bcd-9f13-f177b532d16d

> Inspection records and compliance data for Hirzel Canning Company in Pemberville, Ohio. 4 FDA inspections on record, last inspected September 25, 2019.

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## Details

- Name: Hirzel Canning Company
- FEI Number: 1522299
- Address Line 1: 115 Columbus St
- City: Pemberville
- State: Ohio
- Zip Code: 43450
- Country Name: United States
- Address: 115 Columbus St, Pemberville, Ohio 43450, United States
- Country: United States

## Related Documents

- FDA Inspection 1107823 - Hirzel Canning Company - 2019-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2019
- FDA Inspection 985417 - Hirzel Canning Company - 2016-09-06 — classification: No Action Indicated (NAI), source: FDA, date: September 6, 2016
- FDA Inspection 985417 - Hirzel Canning Company - 2016-09-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 6, 2016
- [FDA Inspection 985417 - Hirzel Canning Company - 2016-09-06](https://www.keypedia.com/records/fda_inspections/hirzel-canning-company/c34a6c26-2f1e-4d32-b8e0-22308fea4576) — classification: No Action Indicated (NAI), source: FDA, date: September 6, 2016
- FDA Inspection 985417 - Hirzel Canning Company - 2016-09-06 — classification: No Action Indicated (NAI), source: FDA, date: September 6, 2016
- [FDA Inspection 848996 - Hirzel Canning Company - 2013-09-18](https://www.keypedia.com/records/fda_inspections/hirzel-canning-company/dfb25b19-d045-45d6-ba71-8410ae19786b) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2013
- FDA Inspection 597428 - Hirzel Canning Company - 2009-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2009
- FDA Inspection 597428 - Hirzel Canning Company - 2009-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2009
- FDA Inspection 597428 - Hirzel Canning Company - 2009-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2009

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