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FDA Inspection 1028786 — KMC Systems, Inc.

KMC Systems, Inc. — FEI 1219738

The FDA completed an inspection of KMC Systems, Inc. on October 5, 2017 in Merrimack, NH. 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
October 5, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Merrimack, NH (United States)

Facility

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FDA data resources