FDA Inspection
Teleflex Medical Tuttlingen GmbHTeleflex Medical Tuttlingen GmbH – FDA Inspection, Nov 5, 2013
Record Details
This FDA Inspection record concerns Teleflex Medical Tuttlingen GmbH, with an inspection on November 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 5, 2013
- Product Type
- Devices
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ID · 740a7480-98cc-4289-95ca-ec837f50cdb4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 858921
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
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Other FDA inspections of Teleflex Medical Tuttlingen GmbH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 4, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Teleflex Medical Tuttlingen GmbH
- FDA Inspection 649050 - 2010-02-04
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