FDA Inspection 1089905 — MDI East, Inc.

MDI East, Inc. — FEI 1000120560

The FDA completed an inspection of MDI East, Inc. on April 30, 2019 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
April 30, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Jaffrey, NH (United States)