994785

Maquet Cardiovascular, LLC — FEI 2242352

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 29, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Wayne, NJ (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1472021 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
1472221 CFR 820.40Procedures not adequately established or maintained
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
310821 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
310921 CFR 820.70(d)Personnel requirements, Lack of or inadequate requirements
313021 CFR 820.100(a)Lack of or inadequate procedures
317021 CFR 820.198(b)Review and evaluation for investigation
317221 CFR 820.198(c)Investigation of device failures
326221 CFR 820.250(a)Statistical techniques - Lack of or inadequate procedures
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation
73121 CFR 803.50(a)(1)Report of Death or Serious Injury
73221 CFR 803.50(a)(2)Individual Report of Malfunction
81221 CFR 803.56Submission of Supplement to Individual Report Within One Month