FDA Inspection 833533 — Mega Motion, Inc.

Mega Motion, Inc. — FEI 3002608037

The FDA completed an inspection of Mega Motion, Inc. on May 21, 2013 in Duryea, PA. 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
May 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Duryea, PA (United States)