# Coborn's Incorporated, Saint Cloud, MN – FDA Inspections

Source: https://www.keypedia.com/companies/coborns-incorporated/c463ea8d-9eab-4a0f-af64-6d206e52eb0f

> Inspection records and compliance data for Coborn's Incorporated in Saint Cloud, Minnesota. 13 FDA inspections on record, last inspected September 16, 2026.

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## Details

- Name: Coborn's Incorporated
- FEI Number: 3004249892
- Address Line 1: 1445 Highway 23 E Bldg B
- City: Saint Cloud
- State: Minnesota
- Zip Code: 56304
- Country Name: United States
- Address: 1445 Highway 23 E Bldg B, Saint Cloud, Minnesota 56304, United States
- Country: United States

## Related Documents

- FDA Inspection 1338908 - Coborn's Incorporated - 2026-09-16 — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2026
- [FDA Inspection 1147620 - Coborn's Incorporated - 2021-08-02](https://www.keypedia.com/records/fda_inspections/coborns-incorporated/17c81d4e-eb07-4974-baaf-a5459f95fa9f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 2, 2021
- FDA Inspection 1096526 - Coborn's Incorporated - 2019-07-10 — source: FDA, date: July 10, 2019
- FDA Inspection 1026775 - Coborn's Incorporated - 2017-09-13 — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2017
- FDA Inspection 1026775 - Coborn's Incorporated - 2017-09-13 — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2017
- FDA Inspection 1023163 - Coborn's Incorporated - 2017-07-20 — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2017
- FDA Inspection 994250 - Coborn's Incorporated - 2016-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2016
- FDA Inspection 936712 - Coborn's Incorporated - 2015-07-31 — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2015
- FDA Inspection 862888 - Coborn's Incorporated - 2014-01-22 — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2014
- FDA Inspection 815495 - Coborn's Incorporated - 2013-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2013

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