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FDA Inspection
•Kedrion S.p.A.•June 27, 2014

Kedrion S.p.A. – FDA Inspection, Jun 27, 2014

Record Details

This FDA Inspection record concerns Kedrion S.p.A., with an inspection on June 27, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Kedrion S.p.A.
Inspection Date
June 27, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 48d2e6ac-d7b2-4881-af8b-75a8a980107b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
907163
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Kedrion S.p.A.

5
DateClassificationOfficeProject area
April 10, 2025Not classifiedOffice of Inspections and Investigations
August 28, 2024Not classifiedOffice of Inspections and Investigations
June 24, 2022VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 16, 2016VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
April 18, 2012VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Kedrion S.p.A.
  • FDA Inspection 1281078 - 2025-04-10
  • FDA Inspection 1254229 - 2024-08-28
  • FDA Inspection 1173210 - 2022-06-24
  • FDA Inspection 990289 - 2016-09-16
  • FDA Inspection 785499 - 2012-04-18

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