# FDA Inspection 628046 - Karl Storz GMBH & Co KG   (KSVEM) - October 29, 2009

Source: https://www.keypedia.com/records/fda_inspections/karl-storz-gmbh-co-kg-ksvem/55bd5353-36ab-4a75-97d7-6c8373ba3cbf
Source feed: FDA_Inspections

> FDA Inspection 628046 for Karl Storz GMBH & Co KG   (KSVEM) on October 29, 2009. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 628046
- Company Name: Karl Storz GMBH & Co KG   (KSVEM)
- Inspection Date: 2009-10-29
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 809270 - 2012-11-28](https://www.keypedia.com/records/fda_inspections/karl-storz-gmbh-co-kg-ksvem/89f51c80-3581-4c97-80ff-67b9c65dfd7f)
- [FDA Inspection 809270 - 2012-11-28](https://www.keypedia.com/records/fda_inspections/karl-storz-gmbh-co-kg-ksvem/af90b247-f857-41aa-9373-30723c5d3416)

Company: https://www.keypedia.com/companies/karl-storz-gmbh-co-kg-ksvem/9dee5d3e-560c-43d2-bc46-ab2dc0fa79fe

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