FDA Inspection 1016985 — EKOM spol. s.r.o.

EKOM spol. s.r.o. — FEI 3005245901

The FDA completed an inspection of EKOM spol. s.r.o. on May 25, 2017 in Piestany. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Piestany (Slovakia)