FDA Inspection 838792 — MDI East, Inc.

MDI East, Inc. — FEI 1000120560

The FDA completed an inspection of MDI East, Inc. on July 2, 2013 in Jaffrey, 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
July 2, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Jaffrey, NH (United States)