# Pharmaceutical Laboratories and Consultants, Inc., Addison, IL – FDA Inspections

Source: https://www.keypedia.com/companies/pharmaceutical-laboratories-and-consultants-inc/85916251-446b-4a71-96f6-3db72df555e8

> Inspection records and compliance data for Pharmaceutical Laboratories and Consultants, Inc. in Addison, Illinois. 4 FDA inspections on record (1 OAI), 1 Form 483, last inspected October 10, 2017.

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## Details

- Name: Pharmaceutical Laboratories and Consultants, Inc.
- FEI Number: 3003982646
- Address Line 1: 1010 W Fullerton Ave Ste H
- City: Addison
- State: Illinois
- Zip Code: 60101
- Country Name: United States
- Address: 1010 W Fullerton Ave Ste H, Addison, Illinois 60101, United States
- Country: United States

## Related Documents

- [FDA Inspection 1028257 - Pharmaceutical Laboratories and Consultants, Inc. - 2017-10-10](https://www.keypedia.com/records/fda_inspections/pharmaceutical-laboratories-and-consultants-inc/210a8bda-58ae-494a-b9b7-ec2b73bdf6c7) — classification: Official Action Indicated (OAI), source: FDA, date: October 10, 2017
- FDA Inspection 869173 - Pharmaceutical Laboratories and Consultants, Inc. - 2014-03-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2014
- FDA Inspection 869173 - Pharmaceutical Laboratories and Consultants, Inc. - 2014-03-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2014
- FDA Inspection 809917 - Pharmaceutical Laboratories and Consultants, Inc. - 2012-12-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 13, 2012
- FDA Inspection 809917 - Pharmaceutical Laboratories and Consultants, Inc. - 2012-12-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 13, 2012
- [FDA Inspection 574204 - Pharmaceutical Laboratories and Consultants, Inc. - 2009-05-21](https://www.keypedia.com/records/fda_inspections/pharmaceutical-laboratories-and-consultants-inc/7f105515-df7f-4c55-9198-8af99547b390) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 21, 2009

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