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FDA Inspection 1028892 — Qualtex Laboratories

Qualtex Laboratories — FEI 3006339676

The FDA completed an inspection of Qualtex Laboratories on September 21, 2017 in San Antonio, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 21, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Antonio, TX (United States)

Facility

Other inspections at this facility

  • 1251335 (NAI Fri Sep 27 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1122001 (NAI Thu Feb 27 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1122019 (NAI Thu Feb 27 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025875 (VAI Fri Sep 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 939930 (NAI Thu Aug 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources