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FDA Inspection
•Aurobindo Pharma Limited•September 17, 2010

Aurobindo Pharma Limited – FDA Inspection, Sep 17, 2010

Record Details

This FDA Inspection record concerns Aurobindo Pharma Limited, with an inspection on September 17, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Aurobindo Pharma Limited
Inspection Date
September 17, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 9cf54b3a-8e21-4051-b7ac-26a4ad57dcff

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
684549
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

1
  1. 21 CFR 211.198(b)(2)Complaint Investigation/Follow-Up Findings

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Aurobindo Pharma Limited

7
DateClassificationOfficeProject area
September 5, 2025OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 9, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 21, 2020VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
March 16, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 16, 2013NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 7 other inspections on the company page
Other documents for Aurobindo Pharma Limited
  • FDA Inspection 1286862 - 2025-09-05
  • FDA Inspection 1241780 - 2023-03-09
  • FDA Inspection 1118385 - 2020-02-21
  • FDA Inspection 1046218 - 2018-03-16
  • FDA Inspection 847151 - 2013-08-16

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