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FDA Inspection 681246 — Howard Instruments Inc

Howard Instruments Inc — FEI 1039865

The FDA completed an inspection of Howard Instruments Inc on September 14, 2010 in Tuscaloosa, AL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 14, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuscaloosa, AL (United States)

Facility

Other inspections at this facility

  • 994382 (VAI Tue Nov 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 801414 (OAI Thu Oct 04 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 552193 (OAI Thu Dec 18 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources