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FDA Inspection 896250 — Lone Star Medical Products, Inc.

Lone Star Medical Products, Inc. — FEI 1627186

The FDA completed an inspection of Lone Star Medical Products, Inc. on September 23, 2014 in Stafford, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 23, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Stafford, TX (United States)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 1203824 (NAI Thu Apr 27 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1057460 (NAI Wed May 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1021325 (NAI Thu May 04 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 793298 (OAI Mon Aug 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 711363 (NAI Thu Feb 24 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources