FDA Inspection
Medisize bvMedisize bv – FDA Inspection, Nov 4, 2010
Record Details
This FDA Inspection record concerns Medisize bv, with an inspection on November 4, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medisize bv
- Inspection Date
- November 4, 2010
- Product Type
- Devices
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ID · ae91b19f-55a1-499b-a4bb-cb77da5d3669
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 700375
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Medisize bv
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 23, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 15, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medisize bv
- FDA Inspection 982629 - 2016-05-23
- FDA Inspection 844546 - 2013-08-15
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