FDA Inspection
Willy Rusch GmbH a div of Teleflex MedicalWilly Rusch GmbH a div of Teleflex Medical – FDA Inspection, Jul 18, 2019
Record Details
This FDA Inspection record concerns Willy Rusch GmbH a div of Teleflex Medical, with an inspection on July 18, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- July 18, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · e07b6928-32d2-451c-aa99-ed54f777407e
Inspection Facts
- Inspection number
- 1146119
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Willy Rusch GmbH a div of Teleflex Medical
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 18, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 21, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Willy Rusch GmbH a div of Teleflex Medical
- FDA Inspection 910418 - 2014-12-18
- FDA Inspection 740152 - 2011-07-21
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