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FDA Inspection 1053386 — FOCUS Laboratories, Inc.

FOCUS Laboratories, Inc. — FEI 3008990081

The FDA completed an inspection of FOCUS Laboratories, Inc. on May 22, 2018 in North Little Rock, AR. 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
May 22, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
North Little Rock, AR (United States)

Facility

Other inspections at this facility

  • 1137462 (VAI Wed Mar 24 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066193 (NAI Tue Aug 28 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1051036 (NAI Thu Apr 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 913332 (OAI Fri Feb 06 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 848304 (OAI Fri Sep 13 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources