# AURORIUM LLC - Inspection Records

Source: https://www.keypedia.com/companies/aurorium-llc/1381f644-a64d-49a5-a1bb-b57426080e7d

> Inspection records and compliance data for AURORIUM LLC in Midlothian, Texas. Access full analysis and detailed observations.

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## Details

- Name: AURORIUM LLC
- FEI Number: 1628757
- City: Midlothian
- State: Texas
- Country Name: United States
- Address Line 1: 500 N 9th St
- Zip Code: 76065
- Business Operations: API MANUFACTURE

## Related Documents

- [FDA Inspection 1306572 - AURORIUM LLC - 2026-03-06](https://www.keypedia.com/records/fda_inspections/aurorium-llc/3e4fb51c-13f7-4f13-9dac-4b25748f615b) — source: FDA, date: March 6, 2026
- [FDA Inspection 1053761 - AURORIUM LLC - 2018-05-14](https://www.keypedia.com/records/fda_inspections/aurorium-llc/7abd1fc5-1e6d-48d7-9d23-d80b718e5704) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 14, 2018
- [FDA Inspection 979363 - AURORIUM LLC - 2016-08-05](https://www.keypedia.com/records/fda_inspections/aurorium-llc/b4e5e4ab-7918-4871-b58d-b3014f878de3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 5, 2016
- [FDA Inspection 979363 - AURORIUM LLC - 2016-08-05](https://www.keypedia.com/records/fda_inspections/aurorium-llc/70433a13-d4ab-45cd-80a5-940a49d9fd34) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 5, 2016
- [FDA Inspection 811550 - AURORIUM LLC - 2012-12-20](https://www.keypedia.com/records/fda_inspections/aurorium-llc/31aaf850-c135-43bd-9e89-13dd536684bb) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2012
- [FDA Inspection 811550 - AURORIUM LLC - 2012-12-20](https://www.keypedia.com/records/fda_inspections/aurorium-llc/22c6a92c-6126-42e4-ae35-26b47044a329) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2012
- [FDA Inspection 665184 - AURORIUM LLC - 2010-06-07](https://www.keypedia.com/records/fda_inspections/aurorium-llc/5771e703-5579-40be-a7d9-aeed25e74164) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2010

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