FDA Inspection 903307 — Coapt LLC

Coapt LLC — FEI 3010605876

The FDA completed an inspection of Coapt LLC on November 14, 2014 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 8 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 14, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Chicago, IL (United States)

Citations

IDCFRDescription
226921 CFR 820.20(a)Quality policy and objectives
229321 CFR 820.20(d)Quality plan
230221 CFR 820.20(e)Quality System Procedures
312721 CFR 820.80(e)Documentation
333121 CFR 820.181DMR - not or inadequately maintained
405921 CFR 820.22Quality Audits - defined intervals
41921 CFR 820.20(b)Lack of or inadequate organizational structure
63021 CFR 803.17Lack of Written MDR Procedures