FDA Inspection 809607 — Encision Inc.

Encision Inc. — FEI 1000117361

The FDA completed an inspection of Encision Inc. on December 7, 2012 in Boulder, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 7, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Boulder, CO (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
312821 CFR 820.90(a)Nonconforming product control
316821 CFR 820.198(a)Complaints
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation