# Genus Lifesciences Inc., Allentown, PA – FDA Inspections

Source: https://www.keypedia.com/companies/genus-lifesciences-inc/ba29ccf4-c220-4a87-ab2e-cd37322d0957

> Inspection records and compliance data for Genus Lifesciences Inc. in Allentown, Pennsylvania. 11 FDA inspections on record (1 OAI), 3 Form 483s, last inspected July 31, 2024.

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## Details

- Name: Genus Lifesciences Inc.
- FEI Number: 3003851100
- Business Operations: FDF MANUFACTURE
- Address Line 1: 514 N 12th St
- City: Allentown
- State: Pennsylvania
- Zip Code: 18102
- Country Name: United States
- Address: 514 N 12th St, Allentown, Pennsylvania 18102, United States
- Country: United States

## Related Documents

- [EIR - Genus Lifesciences Inc. - 2024-07-31](https://www.keypedia.com/records/eir/genus-lifesciences-inc/43448352-a32d-41e8-be5a-c67fa60723b7) — source: FDA, date: July 31, 2024
- [FDA Inspection 1245779 - Genus Lifesciences Inc. - 2024-07-31](https://www.keypedia.com/records/fda_inspections/genus-lifesciences-inc/9697db98-6d97-48ea-89fb-e8365f95a26a) — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2024
- [483 - Genus Lifesciences Inc. - 2019-09-20](https://www.keypedia.com/records/483/genus-lifesciences-inc/c705deab-3810-428e-9d86-946cdbe44d35) — source: FDA, date: September 20, 2019
- [FDA Inspection 1102370 - Genus Lifesciences Inc. - 2019-09-20](https://www.keypedia.com/records/fda_inspections/genus-lifesciences-inc/d4bb2b33-6870-4642-b369-ed0acb422c35) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 20, 2019
- [EIR - Genus Lifesciences Inc. - 2018-11-28](https://www.keypedia.com/records/eir/genus-lifesciences-inc/a170f2ad-0ccf-44f3-a5ee-26099dd790ca) — source: FDA, date: November 28, 2018
- FDA Inspection 1073444 - Genus Lifesciences Inc. - 2018-11-28 — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2018
- [FDA Inspection 1059468 - Genus Lifesciences Inc. - 2018-07-20](https://www.keypedia.com/records/fda_inspections/genus-lifesciences-inc/a4d6f7b0-ead6-480e-a51d-f8d17c27e6d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 20, 2018
- [EIR - Genus Lifesciences Inc. - 2017-09-29](https://www.keypedia.com/records/eir/genus-lifesciences-inc/4601c938-2073-46cd-8af7-5238c32e2425) — source: FDA, date: September 29, 2017
- [FDA Inspection 1027671 - Genus Lifesciences Inc. - 2017-09-29](https://www.keypedia.com/records/fda_inspections/genus-lifesciences-inc/90ff5fd9-ad8e-4d9e-b8ce-a7b1bb6ba553) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 29, 2017
- FDA Inspection 982555 - Genus Lifesciences Inc. - 2016-08-11 — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2016
- FDA Inspection 904539 - Genus Lifesciences Inc. - 2014-10-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 17, 2014
- FDA Inspection 809490 - Genus Lifesciences Inc. - 2012-12-05 — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2012
- FDA Inspection 758947 - Genus Lifesciences Inc. - 2011-12-08 — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2011
- [FDA Inspection 710247 - Genus Lifesciences Inc. - 2011-02-03](https://www.keypedia.com/records/fda_inspections/genus-lifesciences-inc/78cfd71d-5c8c-40d5-9bb9-53c8ee35b7b6) — classification: Official Action Indicated (OAI), source: FDA, date: February 3, 2011

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