# JW North America, Inc. – FDA Inspection, Sep 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/jw-north-america-inc/af46360d-ce8d-40f0-8e4e-7a84b03b4214
Source feed: FDA_Inspections

> FDA inspection 944355 of JW North America, Inc., September 21, 2015. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 944355
- Company Name: JW North America, Inc.
- Inspection Date: 2015-09-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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- [FDA Inspection 1093674 - 2019-06-20](https://www.keypedia.com/records/fda_inspections/jw-north-america-inc/c51f9289-9611-4271-a860-b3ad9705ad0a)
- [FDA Inspection 1026370 - 2017-09-22](https://www.keypedia.com/records/fda_inspections/jw-north-america-inc/f768912b-ba7b-4361-8027-214195be5e2b)

Company: https://www.keypedia.com/companies/jw-north-america-inc/23f83c8a-c0ee-4ad9-a666-da739bc0c792

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