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FDA Inspection 831050 — ARK-LA-TEX Fertility and Reproductive Medicine, PMC

ARK-LA-TEX Fertility and Reproductive Medicine, PMC — FEI 3010600107

The FDA completed an inspection of ARK-LA-TEX Fertility and Reproductive Medicine, PMC on April 26, 2013 in Shreveport, LA. 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
April 26, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Shreveport, LA (United States)

Facility

Other inspections at this facility

  • 1280425 (NAI Fri Aug 29 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1217533 (NAI Wed Aug 23 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1042561 (NAI Thu Nov 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 929590 (NAI Fri May 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources