FDA Inspection 1190592 — Junopacific Inc.

Junopacific Inc. — FEI 3002623849

The FDA completed an inspection of Junopacific Inc. on Nov 15, 2022 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 15, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Minneapolis, MN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures