# JW North America, Inc. – FDA Inspection, Sep 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/jw-north-america-inc/f768912b-ba7b-4361-8027-214195be5e2b
Source feed: FDA_Inspections

> FDA inspection 1026370 of JW North America, Inc., September 22, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026370
- Company Name: JW North America, Inc.
- Inspection Date: 2017-09-22
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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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 944355 - 2015-09-21](https://www.keypedia.com/records/fda_inspections/jw-north-america-inc/af46360d-ce8d-40f0-8e4e-7a84b03b4214)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

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