# The Jel Sert Company - Inspection Records

Source: https://www.keypedia.com/companies/the-jel-sert-company/c9696ffe-98b4-4098-a045-a117b24325e5

> Inspection records and compliance data for The Jel Sert Company in West Chicago, Illinois. 15 FDA inspections on record, last inspected April 10, 2025.

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## Details

- Name: The Jel Sert Company
- FEI Number: 3013302296
- Address Line 1: 501 Conde St
- City: West Chicago
- State: Illinois
- Zip Code: 60185
- Country Name: United States
- Address: 501 Conde St, West Chicago, Illinois 60185, United States
- Country: United States

## Related Documents

- FDA Inspection 1253918 - The Jel Sert Company - 2025-04-10 — source: FDA, date: April 10, 2025
- FDA Inspection 1253918 - The Jel Sert Company - 2025-04-10 — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2025
- FDA Inspection 1253918 - The Jel Sert Company - 2025-04-10 — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2025
- FDA Inspection 1224971 - The Jel Sert Company - 2023-12-06 — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2023
- FDA Inspection 1224971 - The Jel Sert Company - 2023-12-06 — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2023
- FDA Inspection 1201585 - The Jel Sert Company - 2023-03-15 — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2023
- FDA Inspection 1201585 - The Jel Sert Company - 2023-03-15 — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2023
- [FDA Inspection 1177745 - The Jel Sert Company - 2022-08-11](https://www.keypedia.com/records/fda_inspections/the-jel-sert-company/964007cd-7cb8-4185-b0f2-0d0605013867) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2022
- FDA Inspection 1177745 - The Jel Sert Company - 2022-08-11 — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2022
- FDA Inspection 1121570 - The Jel Sert Company - 2020-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2020

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