FDA Inspection 755641 — Abington Reproductive Medicine

Abington Reproductive Medicine — FEI 3005587932

The FDA completed an inspection of Abington Reproductive Medicine on Dec 5, 2011 in Abington, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 5, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Abington, PA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.