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FDA Inspection
•Citieffe Srl•April 21, 2017

Citieffe Srl – FDA Inspection, Apr 21, 2017

Record Details

This FDA Inspection record concerns Citieffe Srl, with an inspection on April 21, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Citieffe Srl
Inspection Date
April 21, 2017
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Sarah A. Hassas (Company Rep)
View Company Profile

ID · 16a56448-5171-4234-9f17-d5aaf6d582c5

Inspection Facts

Inspection number
1015096
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Citieffe Srl

1
DateClassificationOfficeProject area
February 15, 2024VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Citieffe Srl
  • FDA Inspection 1238306 - 2024-02-15

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