# GOODHEW, LLC – FDA Inspection, Jun 25, 2018

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

> FDA inspection 1056841 of GOODHEW, LLC, June 25, 2018. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- 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: 9

## Related Officers

- Issuing Officer

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

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