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FDA Inspection
•Eckert & Ziegler Radiopharma GmbH•August 23, 2019

Eckert & Ziegler Radiopharma GmbH – FDA Inspection, Aug 23, 2019

Record Details

This FDA Inspection record concerns Eckert & Ziegler Radiopharma GmbH, with an inspection on August 23, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Eckert & Ziegler Radiopharma GmbH
Inspection Date
August 23, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jose A. Cruz Gonzalez
View Company Profile

ID · 1f96ae21-ed9b-441d-b126-8a954b4b416e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1100386
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Eckert & Ziegler Radiopharma GmbH

2
DateClassificationOfficeProject area
September 27, 2024Not classifiedOffice of Inspections and Investigations
November 6, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Eckert & Ziegler Radiopharma GmbH
  • FDA Inspection 1290454 - 2024-09-27
  • FDA Inspection 947144 - 2015-11-06

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