# FDA Inspection 747417 - INNOVIEW GMBH - September 08, 2011

Source: https://www.keypedia.com/records/fda_inspections/innoview-gmbh/261b9d43-9b70-416f-ab90-53db61bec414
Source feed: FDA_Inspections

> FDA Inspection 747417 for INNOVIEW GMBH on September 08, 2011. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 747417
- Company Name: INNOVIEW GMBH
- Inspection Date: 2011-09-08
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 747417 - 2011-09-08](https://www.keypedia.com/records/fda_inspections/innoview-gmbh/83942d4a-0ca9-4b13-850c-12056c70b60b)
- [FDA Inspection 567235 - 2009-01-28](https://www.keypedia.com/records/fda_inspections/innoview-gmbh/3cd3f13a-5738-4c0b-8425-3bd47d516851)

Company: https://www.keypedia.com/companies/innoview-gmbh/fa569e43-14d3-4d7c-a5f6-98fc0def440d

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