FDA Inspection
Sandoz GmbHSandoz GmbH – FDA Inspection, Oct 13, 2017
Record Details
This FDA Inspection record concerns Sandoz GmbH, with an inspection on October 13, 2017, issued by the Office of Inspections and Investigations, covering human drugs.
- People
- Scott R. Nichols (Issuing Officer)
- Zhong Li
View Company Profile
ID · 2c70d7a2-c20b-4d4d-b78b-9bb17dca4a43
Inspection Facts
- Inspection number
- 1040853
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Sandoz GmbH
8| Date | Classification | Office | Project area |
|---|---|---|---|
| January 12, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 11, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 2, 2018 | Not classified | Office of Inspections and Investigations | |
| July 5, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 18, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sandoz GmbH
- FDA Inspection 1195376 - 2023-01-12
- FDA Inspection 1205998 - 2022-07-11
- FDA Inspection 1045918 - 2018-03-02
- FDA Inspection 981928 - 2016-07-05
- FDA Inspection 872125 - 2014-03-18
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