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FDA Inspection 1012034 — Spellman Hg Vltg Elctrnc

Spellman Hg Vltg Elctrnc — FEI 2429877

The FDA completed an inspection of Spellman Hg Vltg Elctrnc on April 26, 2017 in Hauppauge, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 26, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Hauppauge, NY (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation

Facility

Other inspections at this facility

  • 867057 (NAI Fri Feb 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 777937 (NAI Tue Apr 17 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 639308 (NAI Fri Jan 15 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources