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FDA Inspection 583033 — Foulk & Whitten Nevada Center For Reproductive Medicine

Foulk & Whitten Nevada Center For Reproductive Medicine — FEI 3004105841

The FDA completed an inspection of Foulk & Whitten Nevada Center For Reproductive Medicine on May 6, 2009 in Reno, NV. 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
May 6, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Reno, NV (United States)

Facility

Other inspections at this facility

  • 1223875 (NAI Wed Nov 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1084676 (VAI Thu Mar 28 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 993202 (VAI Wed Nov 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 883672 (NAI Thu Jun 05 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 727117 (NAI Tue May 31 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources