# SensoryEffects Inc., Faribault, MN – FDA Inspections

Source: https://www.keypedia.com/companies/sensoryeffects-inc/739d8973-5f7d-4ceb-a517-6d185ced334b

> Inspection records and compliance data for SensoryEffects Inc. in Faribault, Minnesota. 10 FDA inspections on record, 1 Form 483, last inspected March 02, 2026.

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## Details

- Name: SensoryEffects Inc.
- FEI Number: 1000306729
- Address Line 1: 2125 Airport Dr
- City: Faribault
- State: Minnesota
- Zip Code: 55021
- Country Name: United States
- Address: 2125 Airport Dr, Faribault, Minnesota 55021, United States
- Country: United States

## Related Documents

- [FDA Inspection 1307524 - SensoryEffects Inc. - 2026-03-02](https://www.keypedia.com/records/fda_inspections/sensoryeffects-inc/85d5b47e-9722-4c33-bd38-b13773716964) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 2, 2026
- [483 - SensoryEffects Inc. - 2020-03-02](https://www.keypedia.com/records/483/sensoryeffects-inc/0960ec9a-3be3-43fe-bdb2-70149e99f68b) — source: FDA, date: March 2, 2020
- FDA Inspection 1077439 - SensoryEffects Inc. - 2019-01-10 — source: FDA, date: January 10, 2019
- FDA Inspection 1025084 - SensoryEffects Inc. - 2017-09-07 — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2017
- FDA Inspection 1025084 - SensoryEffects Inc. - 2017-09-07 — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2017
- FDA Inspection 984208 - SensoryEffects Inc. - 2016-08-23 — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2016
- FDA Inspection 898658 - SensoryEffects Inc. - 2014-09-03 — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2014
- FDA Inspection 844822 - SensoryEffects Inc. - 2013-08-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 23, 2013
- FDA Inspection 748717 - SensoryEffects Inc. - 2011-08-05 — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2011
- FDA Inspection 748717 - SensoryEffects Inc. - 2011-08-05 — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2011
- FDA Inspection 668666 - SensoryEffects Inc. - 2010-06-22 — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2010

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