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FDA Inspection 807674 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3006501046

The FDA completed an inspection of Huntington Reproductive Center Medical Group on November 8, 2012 in Los Angeles, 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
November 8, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Los Angeles, CA (United States)

Facility

Other inspections at this facility

  • 1207182 (NAI Thu Jun 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1043586 (NAI Fri Jan 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 982064 (NAI Tue Feb 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 726254 (VAI Wed May 25 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources