FDA Inspection 1110453 — ELIDAH, INC.

ELIDAH, INC. — FEI 3014915464

The FDA completed an inspection of ELIDAH, INC. on Nov 12, 2019 in Newtown, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 12, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Newtown, CT (United States)

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