# Arthur Schuman Midwest LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/arthur-schuman-midwest-llc/ad202b8c-cf66-47c0-9abe-672a9a516d2b

> Inspection records and compliance data for Arthur Schuman Midwest LLC in Elgin, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Arthur Schuman Midwest LLC
- FEI Number: 3002716362
- City: Elgin
- State: Illinois
- Country Name: United States
- Address Line 1: 2589 Technology Dr
- Zip Code: 60124

## Related Documents

- [FDA Inspection 1109834 - Arthur Schuman Midwest LLC - 2019-11-12](https://www.globalkeysolutions.net/records/fda_inspections/arthur-schuman-midwest-llc/a8686e3a-5d9e-4ef0-966e-4ca440c3f9a5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 12, 2019
- [FDA Inspection 1109834 - Arthur Schuman Midwest LLC - 2019-11-12](https://www.globalkeysolutions.net/records/fda_inspections/arthur-schuman-midwest-llc/d07e05d7-365a-4c8f-8405-de972f13a909) — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2019
- [FDA Inspection 1005240 - Arthur Schuman Midwest LLC - 2017-03-08](https://www.globalkeysolutions.net/records/fda_inspections/arthur-schuman-midwest-llc/22c2817d-5187-47dc-b3fa-2fe5be4a3e75) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 8, 2017
- [FDA Inspection 974409 - Arthur Schuman Midwest LLC - 2016-04-07](https://www.globalkeysolutions.net/records/fda_inspections/arthur-schuman-midwest-llc/fb6f16ad-5a74-45b6-845f-d82b3c94ea85) — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2016
- [FDA Inspection 837535 - Arthur Schuman Midwest LLC - 2013-05-28](https://www.globalkeysolutions.net/records/fda_inspections/arthur-schuman-midwest-llc/3f777145-9bb0-41b9-8329-a83bd200a7a9) — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2013
- [FDA Inspection 823518 - Arthur Schuman Midwest LLC - 2013-03-21](https://www.globalkeysolutions.net/records/fda_inspections/arthur-schuman-midwest-llc/998bc414-4c28-4e46-9f94-c543d81ff588) — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2013

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