FDA Inspection 878747 — Apolo - Megasun LLC

Apolo - Megasun LLC — FEI 3006190476

The FDA completed an inspection of Apolo - Megasun LLC on May 14, 2014 in Saint Louis, MO. 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 14, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Saint Louis, MO (United States)