FDA Inspection
Karl Storz Endoscopy America IncKarl Storz Endoscopy America Inc – FDA Inspection, Jan 5, 2010
Record Details
This FDA Inspection record concerns Karl Storz Endoscopy America Inc, with an inspection on January 5, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 5, 2010
- Product Type
- Devices
View Company Profile
ID · fa809047-772e-4610-b76d-589ca11081f3
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 642593
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Karl Storz Endoscopy America Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 15, 2024 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 24, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 4, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 10, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Karl Storz Endoscopy America Inc
- FDA Inspection 1230647 - 2024-02-15
- FDA Inspection 1170790 - 2022-05-24
- FDA Inspection 1093439 - 2019-06-04
- FDA Inspection 998085 - 2017-01-10
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