FDA Inspection
MEGIN OYMEGIN OY – FDA Inspection, Jul 19, 2012
Record Details
This FDA Inspection record concerns MEGIN OY, with an inspection on July 19, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- MEGIN OY
- Inspection Date
- July 19, 2012
- Product Type
- Devices
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ID · 4927e8f3-5236-4d66-9db2-34c124dc8998
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 794673
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 806.10(a)(1)Report of risk to health
- 21 CFR 820.30(g)Design validation - documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of MEGIN OY
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 27, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for MEGIN OY
- FDA Inspection 995999 - 2016-10-27
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