FDA Inspection 959093 — Degania Medical Devices Pvt. Ltd.

Degania Medical Devices Pvt. Ltd. — FEI 3005483737

The FDA completed an inspection of Degania Medical Devices Pvt. Ltd. on January 21, 2016 in Gurgaon. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 21, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Gurgaon (India)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation