FDA Inspection
Medtronic Vascular Galway DBA Medtronic IrelandFDA Inspection 969068 - Medtronic Vascular Galway DBA Medtronic Ireland - February 12, 2016
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Record Details
This FDA Inspection record concerns Medtronic Vascular Galway DBA Medtronic Ireland, with an inspection on February 12, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 12, 2016
- Product Type
- Devices
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ID · e6fb5200-e5cb-4ffd-b557-cab0ce7c95b1
Violation Codes5
21 CFR 211.160(a)21 CFR 820.70(e)21 CFR 820.70(g)21 CFR 820.70(g)(1)21 CFR 820.80(d)
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