# Aurolife Pharma, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/aurolife-pharma-llc/b82a0c8c-6b52-4624-8c6c-21887615bc7d

> Inspection records and compliance data for Aurolife Pharma, LLC in Dayton, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Aurolife Pharma, LLC
- FEI Number: 3005796917
- City: Dayton
- State: New Jersey
- Country Name: United States
- Address Line 1: 2400 US Highway 130
- Zip Code: 08810
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK, REPACK

## Related Documents

- [483 - Aurolife Pharma, LLC - 2021-12-07](https://www.globalkeysolutions.net/records/483/aurolife-pharma-llc/c6b0115c-7a88-4138-8337-6f7454a491c3) — source: FDA, date: December 7, 2021
- [FDA Inspection 1158258 - Aurolife Pharma, LLC - 2021-12-07](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/b5941257-91bb-4441-8ba8-f35bfcc3ecea) — classification: Official Action Indicated (OAI), source: FDA, date: December 7, 2021
- [483 - Aurolife Pharma, LLC - 2020-02-12](https://www.globalkeysolutions.net/records/483/aurolife-pharma-llc/1c6eef37-2104-432a-93e6-3a687c3d4c8f) — source: FDA, date: February 12, 2020
- [WARNING_LETTER - Aurolife Pharma, LLC - 2020-02-12](https://www.globalkeysolutions.net/records/warning_letter/aurolife-pharma-llc/8d5386ca-53df-44f7-9289-0337abcaf29f) — source: FDA, date: February 12, 2020
- [483 - Aurolife Pharma, LLC - 2019-10-22](https://www.globalkeysolutions.net/records/483/aurolife-pharma-llc/5b283c99-9b47-413e-9caf-15e27bb8a8bf) — source: FDA, date: October 22, 2019
- [FDA Inspection 1109452 - Aurolife Pharma, LLC - 2019-10-22](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/f3f35fbe-6437-47a7-bc74-81e3630b8603) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2019
- [FDA Inspection 1055912 - Aurolife Pharma, LLC - 2018-06-14](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/af02282b-baad-459c-ab27-5f81e3b9e7be) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 14, 2018
- [FDA Inspection 980107 - Aurolife Pharma, LLC - 2016-07-28](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/8bc0e8f0-ab10-4d53-bcb0-434db2cd07a5) — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2016
- [FDA Inspection 952634 - Aurolife Pharma, LLC - 2016-01-12](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/0cebeb11-22eb-46cf-aebd-b3c8e0fcd074) — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2016
- [FDA Inspection 933659 - Aurolife Pharma, LLC - 2015-07-09](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/edba1fb4-b869-428f-8df1-8a57da7f3d3c) — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2015
- [FDA Inspection 851573 - Aurolife Pharma, LLC - 2013-10-15](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/0040e841-dc45-46bb-9a03-d56fc94b4bf4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2013
- [FDA Inspection 752057 - Aurolife Pharma, LLC - 2011-11-02](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/2a993352-9a70-4eeb-a75e-ab898463b93c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 2, 2011
- [FDA Inspection 727943 - Aurolife Pharma, LLC - 2011-05-25](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/df9386a6-7efe-4aac-acde-70fa19ee80b2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 25, 2011
- [FDA Inspection 581003 - Aurolife Pharma, LLC - 2009-05-11](https://www.globalkeysolutions.net/records/fda_inspections/aurolife-pharma-llc/e6160830-41ca-4b8e-bfbd-7d6a3ae4d3c7) — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2009

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