# JK Products & Services, Inc – FDA Inspection, Feb 10, 2012

Source: https://www.keypedia.com/records/fda_inspections/jk-products-services-inc/e0686061-c583-4aea-b719-d9c56b62aee9
Source feed: FDA_Inspections

> FDA inspection 767474 of JK Products & Services, Inc, February 10, 2012. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 767474
- Company Name: JK Products & Services, Inc
- Inspection Date: 2012-02-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1017825 - 2017-02-24
- FDA Inspection 900431 - 2014-09-18
- FDA Inspection 795416 - 2012-01-26
- FDA Inspection 685755 - 2010-09-16

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7