FDA Inspection 838589 — Westchester IVF

Westchester IVF — FEI 3005587387

The FDA completed an inspection of Westchester IVF on June 12, 2013 in White Plains, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 12, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
White Plains, NY (United States)

Citations

IDCFRDescription
1222121 CFR 1271.47(a)Procedures for all other requirements
1224721 CFR 1271.55(d)(2)Accurate, indelible, legible