FDA Inspection 751989 — JMEA Corporation

JMEA Corporation — FEI 3008379509

The FDA completed an inspection of JMEA Corporation on Oct 12, 2011 in Rockville, MD. 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
Oct 12, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rockville, MD (United States)