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FDA Inspection 1013053 — Medi-Fare Drug

Medi-Fare Drug — FEI 3009925820

The FDA completed an inspection of Medi-Fare Drug on April 6, 2017 in Blacksburg, SC. 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
April 6, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Blacksburg, SC (United States)

Facility

Other inspections at this facility

  • 1273309 (OAI Fri Jun 06 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1206514 (VAI Fri May 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 897269 (VAI Fri Sep 12 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 837941 (VAI Fri Jun 21 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817905 (OAI Fri Jan 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources