FDA Inspection 1122828 — Mega Motion, Inc.

Mega Motion, Inc. — FEI 3002608037

The FDA completed an inspection of Mega Motion, Inc. on March 12, 2020 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
March 12, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Duryea, PA (United States)