FDA Inspection 805621 — Albany IVF Fertility and Gynecology PLLC DBA Boston IVF The Albany Center

Albany IVF Fertility and Gynecology PLLC DBA Boston IVF The Albany Center — FEI 3004894521

The FDA completed an inspection of Albany IVF Fertility and Gynecology PLLC DBA Boston IVF The Albany Center on November 2, 2012 in Loudonville, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 2, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Loudonville, NY (United States)

Citations

IDCFRDescription
1222221 CFR 1271.47(a)Design of procedures to ensure compliance