FDA Inspection 1253003 — ER Productions

ER Productions — FEI 3010954165

The FDA completed an inspection of ER Productions on Sep 2, 2024 in Dartford. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 2, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Dartford (United Kingdom)