# Akorn, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/akorn-inc/91871042-8cde-411b-b464-09797e0b23db

> Inspection records and compliance data for Akorn, Inc. in Gurnee, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Akorn, Inc.
- FEI Number: 3003102962
- City: Gurnee
- State: Illinois
- Country Name: United States
- Address Line 1: 5605 Centerpoint Ct Ste A
- Zip Code: 60031

## Related Documents

- [FDA Inspection 1085157 - Akorn, Inc. - 2019-03-05](https://www.keypedia.com/records/fda_inspections/akorn-inc/06d441b4-dfd1-4b39-9cd7-eb33bc7c1996) — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2019
- [483 - Akorn, Inc. - 2018-05-16](https://www.keypedia.com/records/483/akorn-inc/5136e44f-4aca-4b08-9dc5-7fe10577623e) — source: FDA, date: May 16, 2018
- [WARNING_LETTER - Akorn, Inc. - 2018-05-16](https://www.keypedia.com/records/warning_letter/akorn-inc/d07fe095-26cd-49a4-a448-3b6512830353) — source: FDA, date: May 16, 2018
- [FDA Inspection 1012412 - Akorn, Inc. - 2017-03-20](https://www.keypedia.com/records/fda_inspections/akorn-inc/faea5b70-1c3c-4d89-9f2b-ab8462069aeb) — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2017
- [FDA Inspection 1004511 - Akorn, Inc. - 2017-02-13](https://www.keypedia.com/records/fda_inspections/akorn-inc/fc5c2163-096e-437c-9942-0c8c5fabba59) — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2017
- [FDA Inspection 950673 - Akorn, Inc. - 2015-12-18](https://www.keypedia.com/records/fda_inspections/akorn-inc/fbf3f256-7811-4dcc-8f07-3424b0d25ac7) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2015
- [FDA Inspection 950673 - Akorn, Inc. - 2015-12-18](https://www.keypedia.com/records/fda_inspections/akorn-inc/557800b1-a314-4264-b532-b1fcd52912c4) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2015
- [WARNING_LETTER - Akorn, Inc. - 2012-10-02](https://www.keypedia.com/records/warning_letter/akorn-inc/64c1b9d7-84e6-40ae-92cd-c562e847494d) — source: FDA, date: October 2, 2012
- [483 - Akorn, Inc. - 2010-09-17](https://www.keypedia.com/records/483/akorn-inc/d583d7c7-6c57-4ec6-8073-4c21483136b9) — source: FDA, date: September 17, 2010
- [483 - Akorn, Inc. - 2009-11-10](https://www.keypedia.com/records/483/akorn-inc/f60cb2d9-b6f6-4c05-8afa-ee130626e106) — source: FDA, date: November 10, 2009
- [FDA Inspection 629551 - Akorn, Inc. - 2009-11-10](https://www.keypedia.com/records/fda_inspections/akorn-inc/9148056f-03bd-4066-9193-12341fea1825) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2009
- [483 - Akorn, Inc. - 2009-06-30](https://www.keypedia.com/records/483/akorn-inc/d6866295-ee51-4e24-9c6a-65324614527b) — source: FDA, date: June 30, 2009

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## Related Officers

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- [Scott J. Macintire](https://www.keypedia.com/people/scott-j-macintire/ca3dc0d0-ffd3-4d61-bd98-56aa7d8b15af)
- [Quality Program Specialist/Program Analyst](https://www.keypedia.com/people/lequita-mayhew/7c553294-3678-4771-acb4-92c4b8fbc0b1)