# ALS Group USA, Corp - Inspection Records

Source: https://www.keypedia.com/companies/als-group-usa-corp/6d3305d4-76a4-4d57-8ed6-1e636d486309

> Inspection records and compliance data for ALS Group USA, Corp in Torrance, California. Access full analysis and detailed observations.

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## Details

- Name: ALS Group USA, Corp
- FEI Number: 2027219
- City: Torrance
- State: California
- Country Name: United States
- Address Line 1: 3904 Del Amo Blvd Ste 801
- Zip Code: 90503
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [483 - ALS Group USA, Corp - 2023-06-05](https://www.keypedia.com/records/483/als-group-usa-corp/7b63f612-3502-489d-bfad-d05724259da2) — source: FDA, date: June 5, 2023
- [FDA Inspection 1207264 - ALS Group USA, Corp - 2023-06-05](https://www.keypedia.com/records/fda_inspections/als-group-usa-corp/76cf3ca1-c158-4027-82f2-8661490b459e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 5, 2023
- [483 - ALS Group USA, Corp - 2019-01-25](https://www.keypedia.com/records/483/als-group-usa-corp/0724040e-144f-4a1a-9490-c9fa043695b0) — source: FDA, date: January 25, 2019
- [FDA Inspection 1041299 - ALS Group USA, Corp - 2018-02-16](https://www.keypedia.com/records/fda_inspections/als-group-usa-corp/ba612440-473d-46a8-b310-6574e9948d61) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 16, 2018
- [FDA Inspection 883899 - ALS Group USA, Corp - 2014-06-18](https://www.keypedia.com/records/fda_inspections/als-group-usa-corp/c2293740-f625-4aaf-a2bd-d9b005fdb74e) — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2014
- [FDA Inspection 770574 - ALS Group USA, Corp - 2012-03-01](https://www.keypedia.com/records/fda_inspections/als-group-usa-corp/b8c94891-18b7-462c-b46a-b88b817f5af4) — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2012
- [FDA Inspection 643202 - ALS Group USA, Corp - 2010-01-28](https://www.keypedia.com/records/fda_inspections/als-group-usa-corp/025a54b8-a562-4985-926f-ff089bbdae39) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 28, 2010

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