# FDA Inspection 1071829 - JW North America, Inc. - November 15, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/jw-north-america-inc/19fb1cbb-b5d5-4772-b4f1-bab370e2145d
Source feed: FDA_Inspections

> FDA Inspection 1071829 for JW North America, Inc. on November 15, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1071829
- Company Name: JW North America, Inc.
- Inspection Date: 2018-11-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1031326 - 2017-10-25](https://www.globalkeysolutions.net/records/fda_inspections/jw-north-america-inc/4341ac55-f8a0-4695-bbf1-a0a518029840)
- [FDA Inspection 1031326 - 2017-10-25](https://www.globalkeysolutions.net/records/fda_inspections/jw-north-america-inc/1c019f33-414d-42af-9c86-e2cc444aeb5c)

Company: https://www.globalkeysolutions.net/companies/jw-north-america-inc/35c74be6-3edc-4b0e-ba39-2c5e438eb32b

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