FDA Inspection
3Shape Poland3Shape Poland – FDA Inspection, Sep 26, 2013
Record Details
This FDA Inspection record concerns 3Shape Poland, with an inspection on September 26, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- 3Shape Poland
- Inspection Date
- September 26, 2013
- Product Type
- Devices
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ID · 6d937e5f-274e-414a-94c6-02f050dec43b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 851801
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.50(a)(2)Supplier oversight
Full citation text and observation details available on the Dashboard.
Other FDA inspections of 3Shape Poland
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 30, 2017 | Not classified | Office of Inspections and Investigations | Postmarket Assurance: Devices |
Other documents for 3Shape Poland
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