# Intergel  Pharmaceuticals, LLC, Irvington, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/intergel-pharmaceuticals-llc/dea26903-bf97-4337-b7c6-183310a6fb65

> Inspection records and compliance data for Intergel  Pharmaceuticals, LLC in Irvington, New Jersey. 4 FDA inspections on record, 1 Form 483, last inspected November 20, 2018.

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## Details

- Name: Intergel  Pharmaceuticals, LLC
- FEI Number: 1000526797
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE
- Address Line 1: 191 40th St
- City: Irvington
- State: New Jersey
- Zip Code: 07111
- Country Name: United States
- Address: 191 40th St, Irvington, New Jersey 07111, United States
- Country: United States

## Related Documents

- [483 - Intergel  Pharmaceuticals, LLC - 2018-11-20](https://www.keypedia.com/records/483/intergel-pharmaceuticals-llc/98e1ccd4-0d7b-44be-ad24-5da6849f2da9) — source: FDA, date: November 20, 2018
- [FDA Inspection 1074009 - Intergel  Pharmaceuticals, LLC - 2018-11-20](https://www.keypedia.com/records/fda_inspections/intergel-pharmaceuticals-llc/6cc80c24-8465-440d-a2bf-7e0064fa9e93) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2018
- FDA Inspection 998543 - Intergel  Pharmaceuticals, LLC - 2016-12-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 14, 2016
- FDA Inspection 998543 - Intergel  Pharmaceuticals, LLC - 2016-12-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 14, 2016
- FDA Inspection 866307 - Intergel  Pharmaceuticals, LLC - 2014-02-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 11, 2014
- [FDA Inspection 751003 - Intergel  Pharmaceuticals, LLC - 2011-11-14](https://www.keypedia.com/records/fda_inspections/intergel-pharmaceuticals-llc/fe6cbc94-73c4-43a8-a5db-c7554c39577e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 14, 2011
- FDA Inspection 751003 - Intergel  Pharmaceuticals, LLC - 2011-11-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 14, 2011

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