FDA Inspection 1111929 — Degania Medical Devices Pvt. Ltd.

Degania Medical Devices Pvt. Ltd. — FEI 3005483737

The FDA completed an inspection of Degania Medical Devices Pvt. Ltd. on Nov 7, 2019 in Gurgaon. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Nov 7, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Gurgaon (India)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.