# FDA Inspection 1056841 - GOODHEW, LLC - June 25, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/goodhew-llc/d7e8277f-0fea-4a8b-8285-c62ae547422e
Source feed: FDA_Inspections

> FDA Inspection 1056841 for GOODHEW, LLC on June 25, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056841
- Company Name: GOODHEW, LLC
- Inspection Date: 2018-06-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1056841 - 2018-06-25](https://www.globalkeysolutions.net/records/fda_inspections/goodhew-llc/4e33bbb8-526e-463c-bd31-4c2550afcf39)

Company: https://www.globalkeysolutions.net/companies/goodhew-llc/62f9f82b-803b-4006-bea5-c53f16337452

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