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FDA Inspection
•AstraZeneca Pharmaceuticals LP•January 27, 2017

AstraZeneca Pharmaceuticals LP – FDA Inspection, Jan 27, 2017

Record Details

This FDA Inspection record concerns AstraZeneca Pharmaceuticals LP, with an inspection on January 27, 2017, issued by the Baltimore District Office, covering human drugs.

Company
AstraZeneca Pharmaceuticals LP
Inspection Date
January 27, 2017
Product Type
Human Drugs
Office
Baltimore District Office
People
  • Diane L. Raccasi (Issuing Officer)
  • Maria J. Lopez- Barragan (Issuing Officer)
  • Zhong Li
View Company Profile

ID · a0a1d2cb-acc7-4166-bea1-b2603ebcba60

Inspection Facts

Inspection number
1001245
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of AstraZeneca Pharmaceuticals LP

8
DateClassificationOfficeProject area
June 7, 2024Not classifiedBaltimore District Office
January 19, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 26, 2019Not classifiedBaltimore District Office
August 17, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 23, 2017Not classifiedBaltimore District Office
View all 8 other inspections on the company page
Other documents for AstraZeneca Pharmaceuticals LP
  • FDA Inspection 1242118 - 2024-06-07
  • FDA Inspection 1197584 - 2023-01-19
  • FDA Inspection 1103507 - 2019-08-26
  • FDA Inspection 1062666 - 2018-08-17
  • FDA Inspection 1025484 - 2017-05-23

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