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FDA Inspection 1056321 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3009565053

The FDA completed an inspection of Huntington Reproductive Center Medical Group on March 23, 2018 in Newport Beach, 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
March 23, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Newport Beach, CA (United States)

Facility

Other inspections at this facility

  • 1253031 (VAI Tue Oct 29 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1201073 (NAI Tue Mar 28 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941285 (NAI Wed Sep 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources