# FDA Inspection 698534 - KARL STORZ GMBH & CO. KG - October 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/karl-storz-gmbh-co-kg/4e95e8f1-a792-4a59-883a-cb8f2f14f384
Source feed: FDA_Inspections

> FDA Inspection 698534 for KARL STORZ GMBH & CO. KG on October 21, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 698534
- Company Name: KARL STORZ GMBH & CO. KG
- Inspection Date: 2010-10-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 893958 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/karl-storz-gmbh-co-kg/3358e07c-2a2b-4c98-b8e0-0756079ac0f4)

Company: https://www.keypedia.com/companies/karl-storz-gmbh-co-kg/bb1494b4-7aaa-46ae-a7ee-e8fcad02f664

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