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FDA Inspection
•Sandoz GmbH•March 16, 2012

FDA Inspection 773115 - Sandoz GmbH - March 16, 2012

Record Details

This FDA Inspection record concerns Sandoz GmbH, with an inspection on March 16, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Sandoz GmbH
Inspection Date
March 16, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 76b8f730-5ddc-4d91-af3c-e0ae8c8bc41e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
773115
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Sandoz GmbH

6
DateClassificationOfficeProject area
January 12, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
July 11, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 5, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 18, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 29, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Sandoz GmbH
  • FDA Inspection 1195376 - 2023-01-12
  • FDA Inspection 1205998 - 2022-07-11
  • FDA Inspection 981928 - 2016-07-05
  • FDA Inspection 872125 - 2014-03-18
  • FDA Inspection 678670 - 2010-07-29

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