FDA Inspection
Biotronik SE & Co. KGBiotronik SE & Co. KG – FDA Inspection, Feb 8, 2017
Record Details
This FDA Inspection record concerns Biotronik SE & Co. KG, with an inspection on February 8, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Biotronik SE & Co. KG
- Inspection Date
- February 8, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · ca1807b5-cf2d-4a82-a5e0-706a30618bad
Inspection Facts
- Inspection number
- 1005940
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Biotronik SE & Co. KG
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 22, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 10, 2016 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 13, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 18, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 2, 2009 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Biotronik SE & Co. KG
- FDA Inspection 1022011 - 2017-06-22
- FDA Inspection 965124 - 2016-03-10
- FDA Inspection 847640 - 2013-08-13
- FDA Inspection 742999 - 2011-08-18
- FDA Inspection 597351 - 2009-07-02
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