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

Source: https://www.keypedia.com/records/fda_inspections/goodman-company-ltd/ca4798a5-51b5-428f-b04a-1210067df071
Source feed: FDA_Inspections

> FDA inspection 1227867 of Goodman Company, Ltd., January 25, 2024. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1227867
- Company Name: Goodman Company, 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: 3

## Related Documents

- [FDA Inspection 1267718 - 2025-04-10](https://www.keypedia.com/records/fda_inspections/goodman-company-ltd/94245503-5fa5-49b7-aa31-fd08d1d20bd2)

## Related Officers

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

Company: https://www.keypedia.com/companies/goodman-company-ltd/4cc88498-fe05-4ea0-a075-96dc5c6188ed

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