FDA Inspection
Medisize Ireland LtdMedisize Ireland Ltd – FDA Inspection, Jun 24, 2016
Record Details
This FDA Inspection record concerns Medisize Ireland Ltd, with an inspection on June 24, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medisize Ireland Ltd
- Inspection Date
- June 24, 2016
- Product Type
- Devices
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ID · 673662ed-e1f1-4904-8fea-c61c077363e8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 978526
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.90(a)Nonconforming product control
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