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FDA Inspection 1199425 — Sparhawk Laboratories, Inc.

Sparhawk Laboratories, Inc. — FEI 1910619

The FDA completed an inspection of Sparhawk Laboratories, Inc. on February 27, 2023 in Lenexa, KS. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 27, 2023
Fiscal Year
2023
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Lenexa, KS (United States)

Facility

Other inspections at this facility

  • 1276111 (VAI Thu Jul 17 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1272179 (OAI Fri May 09 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1136995 (VAI Tue Mar 23 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1122556 (OAI Fri Feb 28 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1070420 (VAI Mon Oct 29 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources