Home / Inspections / 1016123

FDA Inspection 1016123 — 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 June 29, 2017 in Loudonville, 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 29, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Loudonville, NY (United States)

Citations

IDCFRDescription
1223021 CFR 1271.50(a)Responsible person to determine, document
1249421 CFR 1271.85(c)Reproductive cells or tissues

Facility

Other inspections at this facility

  • 1315880 (NAI Tue Apr 21 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1178670 (NAI Tue Aug 30 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1076634 (NAI Tue Nov 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 894358 (NAI Mon Sep 08 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 805621 (VAI Fri Nov 02 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources