FDA Inspection 800840 — IVF Michigan, P.C.

IVF Michigan, P.C. — FEI 3006524185

The FDA completed an inspection of IVF Michigan, P.C. on Jul 31, 2012 in Dearborn, MI. 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
Jul 31, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Dearborn, MI (United States)

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