# JK Products & Services, Inc, Jonesboro, AR – FDA Inspections

Source: https://www.keypedia.com/companies/jk-products-services-inc/dd6728a0-0f1b-4b8d-be4d-10ae0b1d68ca

> Inspection records and compliance data for JK Products & Services, Inc in Jonesboro, Arkansas. 5 FDA inspections on record, last inspected February 24, 2017.

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## Details

- Name: JK Products & Services, Inc
- FEI Number: 2311923
- Address Line 1: 1 Walter Kratz Dr
- City: Jonesboro
- State: Arkansas
- Zip Code: 72401
- Country Name: United States
- Address: 1 Walter Kratz Dr, Jonesboro, Arkansas 72401, United States
- Country: United States

## Related Documents

- FDA Inspection 1017825 - JK Products & Services, Inc - 2017-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2017
- FDA Inspection 1017825 - JK Products & Services, Inc - 2017-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2017
- FDA Inspection 1017825 - JK Products & Services, Inc - 2017-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2017
- FDA Inspection 900431 - JK Products & Services, Inc - 2014-09-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 18, 2014
- FDA Inspection 900431 - JK Products & Services, Inc - 2014-09-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 18, 2014
- FDA Inspection 767474 - JK Products & Services, Inc - 2012-02-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2012
- [FDA Inspection 767474 - JK Products & Services, Inc - 2012-02-10](https://www.keypedia.com/records/fda_inspections/jk-products-services-inc/e0686061-c583-4aea-b719-d9c56b62aee9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2012
- FDA Inspection 767474 - JK Products & Services, Inc - 2012-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2012
- FDA Inspection 795416 - JK Products & Services, Inc - 2012-01-26 — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2012
- FDA Inspection 685755 - JK Products & Services, Inc - 2010-09-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2010

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