FDA Inspection 729161 — MDI East, Inc.

MDI East, Inc. — FEI 1000120560

The FDA completed an inspection of MDI East, Inc. on May 17, 2011 in Jaffrey, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 17, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Jaffrey, NH (United States)

Citations

IDCFRDescription
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures