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

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

Record Details

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

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

ID · aea285d2-0630-4d58-a4a8-6219560ec5a3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1227866
FDA center
Medical Devices & Rad Health
Project area
Project Evaluation: Devices

FDA Citations

2
  1. 21 CFR 820.100(a)Lack of or inadequate procedures
  2. 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Goodman Co., Ltd. Goodman Research Center

1
DateClassificationOfficeProject area
May 15, 2025NAIBioresearch Monitoring
Other documents for Goodman Co., Ltd. Goodman Research Center
  • FDA Inspection 1274186 - 2025-05-15

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