FDA Inspection 1200705 — Pulse NightClub

Pulse NightClub — FEI 3022575391

The FDA completed an inspection of Pulse NightClub on March 10, 2023 in Philadelphia, 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 10, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Philadelphia, PA (United States)