# Goodman Co., Ltd – FDA Inspection, Jan 25, 2024

Source: https://www.keypedia.com/records/fda_inspections/goodman-co-ltd/d39374d0-2825-4975-bb2a-75f922fd23db
Source feed: FDA_Inspections

> FDA inspection 1227869 of Goodman Co., Ltd, January 25, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1227869
- Company Name: Goodman Co., Ltd
- Inspection Date: 2024-01-25
- 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: 1

## Related Documents

- FDA Inspection 1269122 - 2025-04-03

## Related Officers

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

Company: https://www.keypedia.com/companies/goodman-co-ltd/4350de27-2dee-4d00-888d-de7612a27605

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