# Regis Technologies, Inc. - Inspection Records

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. Access full analysis and detailed observations.

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## Details

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

## 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](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/e507ac3b-bc77-4750-acab-ceee746d1658) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2022
- [FDA Inspection 1091835 - Regis Technologies, Inc. - 2019-04-23](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/347689e9-179b-4ff2-8b9f-b0598eaaf258) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2019
- [FDA Inspection 981668 - Regis Technologies, Inc. - 2016-08-15](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/74872736-2811-4695-b9d5-1718d2b7219a) — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2016
- [FDA Inspection 981668 - Regis Technologies, Inc. - 2016-08-15](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/c8ce5218-1dc1-43ee-93ac-0126f11e89b2) — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2016
- [FDA Inspection 858655 - Regis Technologies, Inc. - 2013-12-17](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/d9ca87bb-6c96-43b7-9704-bda5fdb058b2) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2013
- [FDA Inspection 858655 - Regis Technologies, Inc. - 2013-12-17](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/bc240775-f838-4555-85ee-94d4ca27e4f4) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2013
- [FDA Inspection 774859 - Regis Technologies, Inc. - 2012-03-30](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/59f01d81-d94e-4e61-a8a0-11f8893e37e3) — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2012
- [FDA Inspection 774859 - Regis Technologies, Inc. - 2012-03-30](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/64e8ef1d-eb78-4535-b45e-1f50ac96690c) — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2012
- [FDA Inspection 713864 - Regis Technologies, Inc. - 2011-03-08](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/4c82f5ef-73e8-436e-84c1-b331b2294ae8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 8, 2011
- [FDA Inspection 583267 - Regis Technologies, Inc. - 2009-05-08](https://www.keypedia.com/records/fda_inspections/regis-technologies-inc/9bb6d9ac-3ccc-4bfc-9f40-711269924e53) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 8, 2009

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