# Jane's Dough Premium Foods LLC, Columbus, OH – FDA Inspections

Source: https://www.keypedia.com/companies/janes-dough-premium-foods-llc/ad67910f-15c5-44de-91f6-c60f271b9970

> Inspection records and compliance data for Jane's Dough Premium Foods LLC in Columbus, Ohio. 4 FDA inspections on record, 1 Form 483, last inspected April 20, 2026.

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## Details

- Name: Jane's Dough Premium Foods LLC
- FEI Number: 3004345059
- Address Line 1: 935 Taylor Station Rd
- City: Columbus
- State: Ohio
- Zip Code: 43230
- Country Name: United States
- Address: 935 Taylor Station Rd, Columbus, Ohio 43230, United States
- Country: United States

## Related Documents

- FDA Inspection 1288339 - Jane's Dough Premium Foods LLC - 2026-04-20 — source: FDA, date: April 20, 2026
- FDA Inspection 1232174 - Jane's Dough Premium Foods LLC - 2024-02-27 — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2024
- [FDA Inspection 1027340 - Jane's Dough Premium Foods LLC - 2017-09-29](https://www.keypedia.com/records/fda_inspections/janes-dough-premium-foods-llc/d97183f9-f9da-4632-a20e-8b32ff0f7f6c) — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2017
- FDA Inspection 1027340 - Jane's Dough Premium Foods LLC - 2017-09-29 — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2017
- FDA Inspection 1027340 - Jane's Dough Premium Foods LLC - 2017-09-29 — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2017
- FDA Inspection 1027340 - Jane's Dough Premium Foods LLC - 2017-09-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 29, 2017
- FDA Inspection 701868 - Jane's Dough Premium Foods LLC - 2010-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2010
- FDA Inspection 701868 - Jane's Dough Premium Foods LLC - 2010-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2010
- FDA Inspection 701868 - Jane's Dough Premium Foods LLC - 2010-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2010

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