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FDA Inspection
•Goodman Co., Ltd•January 25, 2024

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

Record Details

This FDA Inspection record concerns Goodman Co., Ltd, with an inspection on January 25, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Goodman Co., Ltd
Inspection Date
January 25, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • John A. Sciacchitano (Company Rep)
View Company Profile

ID · d39374d0-2825-4975-bb2a-75f922fd23db

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1227869
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Goodman Co., Ltd

1
DateClassificationOfficeProject area
April 3, 2025NAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Goodman Co., Ltd
  • FDA Inspection 1269122 - 2025-04-03

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