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FDA Inspection
•Sandoz GmbH•April 30, 2015

FDA Inspection 938136 - Sandoz GmbH - April 30, 2015

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Record Details

This FDA Inspection record concerns Sandoz GmbH, with an inspection on April 30, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Sandoz GmbH
Inspection Date
April 30, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
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ID · ae3cacb5-363b-4691-8c19-caa7971d0cdc

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
938136
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Sandoz GmbH

9
DateClassificationOfficeProject area
November 17, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 18, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 17, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
January 29, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
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