# Dujo Logos Inc, Princeton, MN – FDA Inspections

Source: https://www.keypedia.com/companies/dujo-logos-inc/bfeb301a-d3f5-4eb7-83fd-63537b6ff77f

> Inspection records and compliance data for Dujo Logos Inc in Princeton, Minnesota. 6 FDA inspections on record, last inspected September 16, 2026.

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## Details

- Name: Dujo Logos Inc
- FEI Number: 2183585
- Address Line 1: 12535 316th Ave
- City: Princeton
- State: Minnesota
- Zip Code: 55371
- Country Name: United States
- Address: 12535 316th Ave, Princeton, Minnesota 55371, United States
- Country: United States

## Related Documents

- FDA Inspection 1338266 - Dujo Logos Inc - 2026-09-16 — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2026
- FDA Inspection 1338266 - Dujo Logos Inc - 2026-09-16 — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2026
- [483 - Dujo Logos Inc - 2022-06-02](https://www.keypedia.com/records/483/dujo-logos-inc/7483860c-4b5d-428a-8a14-eed28b81a1a4) — source: FDA, date: June 2, 2022
- FDA Inspection 1172530 - Dujo Logos Inc - 2022-06-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 2, 2022
- FDA Inspection 1172530 - Dujo Logos Inc - 2022-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2022
- [FDA Inspection 1038139 - Dujo Logos Inc - 2018-01-04](https://www.keypedia.com/records/fda_inspections/dujo-logos-inc/f2234739-760d-4e50-9c16-ff1d76a4e739) — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2018
- FDA Inspection 1038139 - Dujo Logos Inc - 2018-01-04 — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2018
- FDA Inspection 937609 - Dujo Logos Inc - 2015-06-24 — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2015
- FDA Inspection 766353 - Dujo Logos Inc - 2012-02-06 — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2012
- FDA Inspection 647582 - Dujo Logos Inc - 2010-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2010

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