# 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 for Sandoz GmbH on January 12, 2023. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195376 - 2023-01-12](https://www.keypedia.com/records/fda_inspections/sandoz-gmbh/377bd60d-df87-42af-b11a-9634a9bad492)
- [FDA Inspection 1205998 - 2022-07-11](https://www.keypedia.com/records/fda_inspections/sandoz-gmbh/889b53d5-b057-481a-8428-fd8bfea0c303)
- [FDA Inspection 981928 - 2016-07-05](https://www.keypedia.com/records/fda_inspections/sandoz-gmbh/e244ae75-1574-4c09-a0a1-018410843080)
- [FDA Inspection 981928 - 2016-07-05](https://www.keypedia.com/records/fda_inspections/sandoz-gmbh/1f3bae5c-a5e3-4060-9013-b6d0e7a3b552)
- [FDA Inspection 872125 - 2014-03-18](https://www.keypedia.com/records/fda_inspections/sandoz-gmbh/2733eb87-039d-4d97-9d0e-3ce75e7ef05d)

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