# Airistar Technologies LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/airistar-technologies-llc/1297616b-14d6-4a28-a289-29d2e2143be2

> Inspection records and compliance data for Airistar Technologies LLC in Waukegan, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Airistar Technologies LLC
- FEI Number: 3005583594
- City: Waukegan
- State: Illinois
- Country Name: United States
- Address Line 1: 2340 Ernie Krueger Cir
- Zip Code: 60087

## Related Documents

- [FDA Inspection 1060745 - Airistar Technologies LLC - 2018-07-11](https://www.globalkeysolutions.net/records/fda_inspections/airistar-technologies-llc/9e9060db-05c3-43a8-8c8d-f8bcbbf810eb) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2018
- [FDA Inspection 1060745 - Airistar Technologies LLC - 2018-07-11](https://www.globalkeysolutions.net/records/fda_inspections/airistar-technologies-llc/b3321b4c-8caa-4719-843b-90cb787bce31) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2018
- [FDA Inspection 917104 - Airistar Technologies LLC - 2015-03-03](https://www.globalkeysolutions.net/records/fda_inspections/airistar-technologies-llc/e09060c1-7509-4893-b094-529edcbc0ada) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2015
- [FDA Inspection 917104 - Airistar Technologies LLC - 2015-03-03](https://www.globalkeysolutions.net/records/fda_inspections/airistar-technologies-llc/581e0538-3696-4eed-a822-085d343fb3b7) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2015
- [FDA Inspection 741934 - Airistar Technologies LLC - 2011-08-30](https://www.globalkeysolutions.net/records/fda_inspections/airistar-technologies-llc/b11fb648-3b58-4fa4-acfe-d4273297fd1d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 30, 2011
- [FDA Inspection 741934 - Airistar Technologies LLC - 2011-08-30](https://www.globalkeysolutions.net/records/fda_inspections/airistar-technologies-llc/cc79a182-0a6f-4559-a912-772e081cc052) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 30, 2011

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