FDA Inspection 1026610 — M&S Technologies

M&S Technologies — FEI 1000431353

The FDA completed an inspection of M&S Technologies on September 7, 2017 in Niles, IL. 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
September 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Niles, IL (United States)