# Karl Storz SE & Co. KG – FDA Inspection, Oct 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/karl-storz-se-co-kg/e012eb6c-9ecb-4c95-85d0-16561b475b66
Source feed: FDA_Inspections

> FDA inspection 807643 of Karl Storz SE & Co. KG, October 18, 2012. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 807643
- Company Name: Karl Storz SE & Co. KG
- Inspection Date: 2012-10-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1194478 - 2022-10-13](https://www.keypedia.com/records/fda_inspections/karl-storz-se-co-kg/30166722-bb3a-4c79-9330-7bbad31cc2c1)
- FDA Inspection 1121364 - 2020-03-12
- [FDA Inspection 1018675 - 2017-03-16](https://www.keypedia.com/records/fda_inspections/karl-storz-se-co-kg/2f05ae9d-c729-40ff-8280-44c21a33ed2f)
- FDA Inspection 647961 - 2010-02-04

Company: https://www.keypedia.com/companies/karl-storz-se-co-kg/9a3c2a81-9936-4f85-bc12-6ac095561af9

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