# Aurora Pharmaceutical, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/aurora-pharmaceutical-inc/856a280c-c54c-459b-bccd-1cca8ef4203d

> Inspection records and compliance data for Aurora Pharmaceutical, Inc. in Northfield, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Aurora Pharmaceutical, Inc.
- FEI Number: 3008276347
- City: Northfield
- State: Minnesota
- Country Name: United States
- Address Line 1: 1196 Highway 3 S
- Zip Code: 55057

## Related Documents

- [WARNING_LETTER - Aurora Pharmaceutical, Inc. - 2025-03-11](https://www.keypedia.com/records/warning_letter/aurora-pharmaceutical-inc/9f2a86f7-4afa-4597-8bb9-f7a8163b5ac1) — source: FDA, date: March 11, 2025
- [FDA Inspection 1231561 - Aurora Pharmaceutical, Inc. - 2024-01-19](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/f6a89360-6412-4a2a-bc14-688233927a94) — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2024
- [FDA Inspection 1231561 - Aurora Pharmaceutical, Inc. - 2024-01-19](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/944b8d00-408a-4d39-a51c-3bf87e96b055) — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2024
- [FDA Inspection 1075565 - Aurora Pharmaceutical, Inc. - 2018-11-27](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/61660fe7-b580-484c-bba4-6688efb7bd76) — classification: No Action Indicated (NAI), source: FDA, date: November 27, 2018
- [FDA Inspection 1075565 - Aurora Pharmaceutical, Inc. - 2018-11-27](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/773d0a36-055a-45b0-ad5b-c29c96c72ad3) — classification: No Action Indicated (NAI), source: FDA, date: November 27, 2018
- [FDA Inspection 995344 - Aurora Pharmaceutical, Inc. - 2016-10-17](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/8396040e-dd2b-4125-a51a-7773430ba37d) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2016
- [FDA Inspection 995344 - Aurora Pharmaceutical, Inc. - 2016-10-17](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/b8e7b3ff-4488-47e0-97fc-789a715b6bde) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2016
- [FDA Inspection 918661 - Aurora Pharmaceutical, Inc. - 2015-03-19](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/322453fe-03b8-43df-a7ee-0a9cb107f7d8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 19, 2015
- [FDA Inspection 811693 - Aurora Pharmaceutical, Inc. - 2012-11-27](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/298fd655-6869-46d6-88f2-a7577805a2ed) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 27, 2012
- [FDA Inspection 718236 - Aurora Pharmaceutical, Inc. - 2011-04-04](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/040d3f74-8247-4f0f-8aa1-265d4fb2d09a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2011
- [FDA Inspection 655830 - Aurora Pharmaceutical, Inc. - 2010-03-23](https://www.keypedia.com/records/fda_inspections/aurora-pharmaceutical-inc/f262b53e-b48d-4e19-9314-b6fab27b346a) — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2010

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