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FDA Inspection
•Hospira Zagreb d.o.o.•March 22, 2019

Hospira Zagreb d.o.o. – FDA Inspection, Mar 22, 2019

Record Details

This FDA Inspection record concerns Hospira Zagreb d.o.o., with an inspection on March 22, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Hospira Zagreb d.o.o.
Inspection Date
March 22, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA DavisM (Issuing Officer)
View Company Profile

ID · 53387c32-9209-49d8-9c4d-defc024a571e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1123692
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Hospira Zagreb d.o.o.

3
DateClassificationOfficeProject area
November 7, 2023NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
December 16, 2021NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 20, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Hospira Zagreb d.o.o.
  • FDA Inspection 1225278 - 2023-11-07
  • FDA Inspection 1226933 - 2021-12-16
  • FDA Inspection 1051780 - 2018-02-20

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