1015370

Biolife, LLC — FEI 3003395204

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sarasota, FL (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
316821 CFR 820.198(a)Complaints
63021 CFR 803.17Lack of Written MDR Procedures