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FDA Inspection 1021325 — Lone Star Medical Products, Inc.

Lone Star Medical Products, Inc. — FEI 1627186

The FDA completed an inspection of Lone Star Medical Products, Inc. on May 4, 2017 in Stafford, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 4, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Stafford, TX (United States)

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))
  • 896250 (VAI Tue Sep 23 2014 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