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FDA Inspection
•Ionisos S.A.S.•April 5, 2024

FDA Inspection 1237221 - Ionisos S.A.S. - April 05, 2024

Record Details

This FDA Inspection record concerns Ionisos S.A.S., with an inspection on April 5, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Ionisos S.A.S.
Inspection Date
April 5, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Stephen D. Eich (Company Rep)
View Company Profile

ID · 75f0afe5-3bd8-420e-8fc1-48e29c9943ba

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1237221
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Ionisos S.A.S.

1
DateClassificationOfficeProject area
July 3, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Ionisos S.A.S.
  • FDA Inspection 838583 - 2013-07-03

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