# FDA Inspection 1016943 - GAMBRO ROSTOCK GMBH - July 06, 2017

Source: https://www.keypedia.com/records/fda_inspections/gambro-rostock-gmbh/1bf34f56-d267-460c-8078-e913db5febe4
Source feed: FDA_Inspections

> FDA Inspection 1016943 for GAMBRO ROSTOCK GMBH on July 06, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016943
- Company Name: GAMBRO ROSTOCK GMBH
- Inspection Date: 2017-07-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1016943 - 2017-07-06](https://www.keypedia.com/records/fda_inspections/gambro-rostock-gmbh/08e8b7e3-2df5-4f79-b144-7f22bddc7baa)

Company: https://www.keypedia.com/companies/gambro-rostock-gmbh/7632ac20-f238-4e1a-b68a-a0afc62b0d4f

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