1062290

Entrotech Life Sciences, Inc. — FEI 3011393407

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)

Citations

IDCFRDescription
265021 CFR 820.30(f)Design verification - Lack of or inadequate procedures
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
54621 CFR 820.75(a)Lack of or inadequate process validation