# Indilab, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/indilab-inc/f9eaad19-45e3-4ded-a668-1baa2bebbc52

> Inspection records and compliance data for Indilab, Inc. in Franklin Park, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Indilab, Inc.
- FEI Number: 1450962
- City: Franklin Park
- State: Illinois
- Country Name: United States
- Address Line 1: 10367 Franklin Ave
- Zip Code: 60131

## Related Documents

- [483 - Indilab, Inc. - 2026-02-09](https://www.keypedia.com/records/483/indilab-inc/5a362ef7-70fd-4981-a696-c63e65e9321f) — source: FDA, date: February 9, 2026
- [FDA Inspection 1302198 - Indilab, Inc. - 2026-02-09](https://www.keypedia.com/records/fda_inspections/indilab-inc/408cf07d-3cfb-4f92-8dc8-02305cfdda9b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 9, 2026
- [FDA Inspection 1302198 - Indilab, Inc. - 2026-02-09](https://www.keypedia.com/records/fda_inspections/indilab-inc/0ac23763-0b99-4420-8ac5-e21a144ecab1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 9, 2026
- [FDA Inspection 1191439 - Indilab, Inc. - 2022-11-01](https://www.keypedia.com/records/fda_inspections/indilab-inc/0291912c-90c7-4859-ae87-69202d2cac55) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2022
- [FDA Inspection 1191439 - Indilab, Inc. - 2022-11-01](https://www.keypedia.com/records/fda_inspections/indilab-inc/cee97d59-e632-419c-91a0-aab01a7df431) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2022
- [FDA Inspection 1073332 - Indilab, Inc. - 2018-11-28](https://www.keypedia.com/records/fda_inspections/indilab-inc/1e1b074a-44a2-4e1d-accf-a0d527f3e683) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2018
- [FDA Inspection 1073332 - Indilab, Inc. - 2018-11-28](https://www.keypedia.com/records/fda_inspections/indilab-inc/acfaaea2-c85e-4af3-bfea-92ddcdbab2bd) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2018
- [FDA Inspection 991812 - Indilab, Inc. - 2016-11-07](https://www.keypedia.com/records/fda_inspections/indilab-inc/618f82ff-e48c-4cd9-bac8-38fe4434e3fd) — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2016
- [FDA Inspection 991812 - Indilab, Inc. - 2016-11-07](https://www.keypedia.com/records/fda_inspections/indilab-inc/d823db20-b6b3-47c6-856d-f69b35f90ffd) — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2016
- [FDA Inspection 837256 - Indilab, Inc. - 2013-06-24](https://www.keypedia.com/records/fda_inspections/indilab-inc/eb83fb46-6fcf-401e-a64a-d0f45504fc50) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2013
- [FDA Inspection 837256 - Indilab, Inc. - 2013-06-24](https://www.keypedia.com/records/fda_inspections/indilab-inc/2989c6ee-27fe-4cfb-b874-21c353d3a16f) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2013

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## Related Officers

- [Medical Device Specialist](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)
