FDA Inspection
Karl Storz SE & Co. KGKarl Storz SE & Co. KG – FDA Inspection, Mar 16, 2017
Record Details
This FDA Inspection record concerns Karl Storz SE & Co. KG, with an inspection on March 16, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Karl Storz SE & Co. KG
- Inspection Date
- March 16, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 2f05ae9d-c729-40ff-8280-44c21a33ed2f
Inspection Facts
- Inspection number
- 1018675
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Karl Storz SE & Co. KG
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 13, 2022 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 12, 2020 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 18, 2012 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 4, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Karl Storz SE & Co. KG
- FDA Inspection 1194478 - 2022-10-13
- FDA Inspection 1121364 - 2020-03-12
- FDA Inspection 807643 - 2012-10-18
- FDA Inspection 647961 - 2010-02-04
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