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FDA Inspection 675342 — Sofie Co

Sofie Co — FEI 3004977184

The FDA completed an inspection of Sofie Co on August 11, 2010 in Sterling, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 11, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sterling, VA (United States)

Facility

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  • 1073264 (VAI Mon Dec 03 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 924228 (NAI Fri Jan 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817083 (VAI Fri Feb 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources