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FDA Inspection 985378 — Newport Beach IVF, LLC

Newport Beach IVF, LLC — FEI 3003942657

The FDA completed an inspection of Newport Beach IVF, LLC on September 1, 2016 in Newport Beach, CA. 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 1, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Newport Beach, CA (United States)

Facility

Other inspections at this facility

  • 1225580 (NAI Wed Dec 13 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1102784 (NAI Thu Jul 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 819387 (VAI Tue Feb 26 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 696941 (NAI Fri Oct 29 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources