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FDA Inspection 696941 — Newport Beach IVF, LLC

Newport Beach IVF, LLC — FEI 3003942657

The FDA completed an inspection of Newport Beach IVF, LLC on October 29, 2010 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
October 29, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Newport Beach, CA (United States)

Facility

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FDA data resources