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FDA Inspection 571281 — Center for Reproductive Health Fertility Laboratory of Nashville

Center for Reproductive Health Fertility Laboratory of Nashville — FEI 3005057005

The FDA completed an inspection of Center for Reproductive Health Fertility Laboratory of Nashville on February 13, 2009 in Nashville, TN. 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 13, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Nashville, TN (United States)

Facility

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FDA data resources