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FDA Inspection
•AstraZeneca UK Ltd.•September 22, 2017

AstraZeneca UK Ltd. – FDA Inspection, Sep 22, 2017

Record Details

This FDA Inspection record concerns AstraZeneca UK Ltd., with an inspection on September 22, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
AstraZeneca UK Ltd.
Inspection Date
September 22, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Doan N. Singh (Issuing Officer)
View Company Profile

ID · 6fad3859-eec2-4184-9e0c-a44c332e56f7

Inspection Facts

Inspection number
1030226
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of AstraZeneca UK Ltd.

6
DateClassificationOfficeProject area
April 27, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 23, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 13, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 11, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 16, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for AstraZeneca UK Ltd.
  • FDA Inspection 1274179 - 2023-04-27
  • FDA Inspection 1129231 - 2020-02-23
  • FDA Inspection 1017549 - 2017-04-13
  • FDA Inspection 878183 - 2014-04-11
  • FDA Inspection 785250 - 2012-03-16

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