FDA Inspection 989624 — Capsule Tech, Inc

Capsule Tech, Inc — FEI 3012302658

The FDA completed an inspection of Capsule Tech, Inc on Oct 20, 2016 in Milford, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 20, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Milford, CT (United States)

Citations

IDCFRDescription
315921 CFR 820.184DHR content