# Regis Technologies, Inc., Morton Grove, IL – FDA Inspections

Source: https://www.keypedia.com/companies/regis-technologies-inc/b28a19bd-2caa-4023-9b89-ee609c032939

> Inspection records and compliance data for Regis Technologies, Inc. in Morton Grove, Illinois. 7 FDA inspections on record, last inspected November 16, 2022.

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## Details

- Name: Regis Technologies, Inc.
- FEI Number: 1416120
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING, PACK
- Address Line 1: 8210 Austin Ave
- City: Morton Grove
- State: Illinois
- Zip Code: 60053
- Country Name: United States
- Address: 8210 Austin Ave, Morton Grove, Illinois 60053, United States
- Country: United States

## Related Documents

- [483 - Regis Technologies, Inc. - 2022-11-16](https://www.keypedia.com/records/483/regis-technologies-inc/6de1b7f6-ab85-4578-8d83-6e955401ace2) — source: FDA, date: November 16, 2022
- FDA Inspection 1193468 - Regis Technologies, Inc. - 2022-11-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2022
- FDA Inspection 1091835 - Regis Technologies, Inc. - 2019-04-23 — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2019
- FDA Inspection 981668 - Regis Technologies, Inc. - 2016-08-15 — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2016
- FDA Inspection 981668 - Regis Technologies, Inc. - 2016-08-15 — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2016
- FDA Inspection 858655 - Regis Technologies, Inc. - 2013-12-17 — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2013
- FDA Inspection 858655 - Regis Technologies, Inc. - 2013-12-17 — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2013
- FDA Inspection 774859 - Regis Technologies, Inc. - 2012-03-30 — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2012
- FDA Inspection 774859 - Regis Technologies, Inc. - 2012-03-30 — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2012
- FDA Inspection 713864 - Regis Technologies, Inc. - 2011-03-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 8, 2011
- FDA Inspection 583267 - Regis Technologies, Inc. - 2009-05-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 8, 2009

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