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FDA Inspection 1199962 — Fisher Wallace Laboratories Inc.

Fisher Wallace Laboratories Inc. — FEI 3006258094

The FDA completed an inspection of Fisher Wallace Laboratories Inc. on March 15, 2023 in Brooklyn, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 15, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brooklyn, NY (United States)

Facility

Other inspections at this facility

  • 1269731 (VAI Tue May 13 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1141346 (NAI Tue Jun 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969525 (VAI Tue Mar 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 909300 (VAI Tue Jan 06 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 812027 (VAI Thu Dec 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources