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FDA Inspection 820873 — Qualtex Laboratories

Qualtex Laboratories — FEI 3006339676

The FDA completed an inspection of Qualtex Laboratories on February 19, 2013 in San Antonio, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 19, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
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))
  • 1028892 (NAI Thu Sep 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025875 (VAI Fri Sep 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources