# SensoryEffects Inc. - Inspection Records

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

> Inspection records and compliance data for SensoryEffects Inc. in Faribault, Minnesota. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1307524 - SensoryEffects Inc. - 2026-03-02](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/85d5b47e-9722-4c33-bd38-b13773716964) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 2, 2026
- [FDA Inspection 1025084 - SensoryEffects Inc. - 2017-09-07](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/e51aedc9-98ba-4663-8e5c-c94c95d25331) — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2017
- [FDA Inspection 1025084 - SensoryEffects Inc. - 2017-09-07](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/53b265f4-fe5d-4412-9857-b3e3f37e0882) — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2017
- [FDA Inspection 984208 - SensoryEffects Inc. - 2016-08-23](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/70803ff4-aee1-4330-92be-5cf75c411cc5) — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2016
- [FDA Inspection 898658 - SensoryEffects Inc. - 2014-09-03](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/25fbf807-5836-4ed4-8e43-c70df75ec593) — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2014
- [FDA Inspection 844822 - SensoryEffects Inc. - 2013-08-23](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/5cbed076-08a3-467d-a35f-b1c66cadb75a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 23, 2013
- [FDA Inspection 748717 - SensoryEffects Inc. - 2011-08-05](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/2fda009c-e224-49e9-9cca-2e7f7e6b7494) — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2011
- [FDA Inspection 748717 - SensoryEffects Inc. - 2011-08-05](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/ec45371e-85db-400e-adfd-7f6108873c21) — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2011
- [FDA Inspection 668666 - SensoryEffects Inc. - 2010-06-22](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/2ac36390-6494-4ef3-b7a6-9c9734bdfa55) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2010
- [FDA Inspection 662185 - SensoryEffects Inc. - 2010-05-20](https://www.globalkeysolutions.net/records/fda_inspections/sensoryeffects-inc/a30991d5-73d0-4e24-b417-aa169e16eaf2) — classification: No Action Indicated (NAI), source: FDA, date: May 20, 2010

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