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FDA Inspection
•Go Medical Industries Pty., Ltd.•June 21, 2017

Go Medical Industries Pty., Ltd. – FDA Inspection, Jun 21, 2017

Record Details

This FDA Inspection record concerns Go Medical Industries Pty., Ltd., with an inspection on June 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Go Medical Industries Pty., Ltd.
Inspection Date
June 21, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Roy Baby (Company Rep)
View Company Profile

ID · a0c22cf8-5d02-4c4c-877b-dc7b30da22bf

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1014898
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 803.50(a)(2)Individual Report of Malfunction
  2. 21 CFR 820.70(a)Production processes

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Go Medical Industries Pty., Ltd.

3
DateClassificationOfficeProject area
December 10, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
February 18, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
September 14, 2011OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Go Medical Industries Pty., Ltd.
  • FDA Inspection 1258046 - 2024-12-10
  • FDA Inspection 917407 - 2015-02-18
  • FDA Inspection 749478 - 2011-09-14

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