# FDA Inspection 900431 - JK Products & Services, Inc - September 18, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/jk-products-services-inc/48c8cd72-88d2-4f1d-a8c6-8a10600ce2c4
Source feed: FDA_Inspections

> FDA Inspection 900431 for JK Products & Services, Inc on September 18, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900431
- Company Name: JK Products & Services, Inc
- Inspection Date: 2014-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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