1066292

Vitrolife Inc. — FEI 3002757762

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
421221 CFR 806.20(b)(4)Justification for not reporting