# Jones Medical Instrument Co., Oak Brook, IL – FDA Inspections

Source: https://www.keypedia.com/companies/jones-medical-instrument-co/ef155956-ca37-4294-87d5-392a791f08bc

> Inspection records and compliance data for Jones Medical Instrument Co. in Oak Brook, Illinois. 6 FDA inspections on record, last inspected October 15, 2026.

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## Details

- Name: Jones Medical Instrument Co.
- FEI Number: 1416588
- Address Line 1: 200 Windsor Dr
- City: Oak Brook
- State: Illinois
- Zip Code: 60523
- Country Name: United States
- Address: 200 Windsor Dr, Oak Brook, Illinois 60523, United States
- Country: United States

## Related Documents

- FDA Inspection 1342212 - Jones Medical Instrument Co. - 2026-10-15 — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2026
- FDA Inspection 1271688 - Jones Medical Instrument Co. - 2025-05-21 — source: FDA, date: May 21, 2025
- FDA Inspection 1271688 - Jones Medical Instrument Co. - 2025-05-21 — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2025
- FDA Inspection 1271688 - Jones Medical Instrument Co. - 2025-05-21 — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2025
- FDA Inspection 1028932 - Jones Medical Instrument Co. - 2017-09-19 — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2017
- FDA Inspection 1028932 - Jones Medical Instrument Co. - 2017-09-19 — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2017
- FDA Inspection 903227 - Jones Medical Instrument Co. - 2014-11-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 13, 2014
- FDA Inspection 903227 - Jones Medical Instrument Co. - 2014-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2014
- FDA Inspection 805545 - Jones Medical Instrument Co. - 2012-10-09 — classification: No Action Indicated (NAI), source: FDA, date: October 9, 2012
- FDA Inspection 805545 - Jones Medical Instrument Co. - 2012-10-09 — classification: No Action Indicated (NAI), source: FDA, date: October 9, 2012

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