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FDA Inspection
•Vasorum Limited•October 19, 2017

Vasorum Limited – FDA Inspection, Oct 19, 2017

Record Details

This FDA Inspection record concerns Vasorum Limited, with an inspection on October 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Vasorum Limited
Inspection Date
October 19, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Maida Henesian (Company Rep)
View Company Profile

ID · 74796de2-55cd-4ce6-a524-3e11cdf36a75

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1030840
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Vasorum Limited

1
DateClassificationOfficeProject area
January 26, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Vasorum Limited
  • FDA Inspection 1199980 - 2023-01-26

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