# FDA Inspection 1195376 - Sandoz GmbH - January 12, 2023

Source: https://www.keypedia.com/records/fda_inspections/sandoz-gmbh/86f9ab67-a44d-428b-83c7-1fbe20ed1b1e
Source feed: FDA_Inspections

> FDA inspection 1195376 of Sandoz GmbH, January 12, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195376
- Company Name: Sandoz GmbH
- Inspection Date: 2023-01-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1205998 - 2022-07-11
- [FDA Inspection 981928 - 2016-07-05](https://www.keypedia.com/records/fda_inspections/sandoz-gmbh/e244ae75-1574-4c09-a0a1-018410843080)
- FDA Inspection 872125 - 2014-03-18
- FDA Inspection 773115 - 2012-03-16
- FDA Inspection 678670 - 2010-07-29

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maryam-tabatabaie/b792042d-e296-446d-90a9-d30c8f635506)

Company: https://www.keypedia.com/companies/sandoz-gmbh/02a3eaeb-a765-43ae-873b-93d1d1523696

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7