FDA Inspection 1010708 — IVF Michigan

IVF Michigan — FEI 3010929692

The FDA completed an inspection of IVF Michigan on Mar 24, 2017 in Bloomfield Hills, 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
Mar 24, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Bloomfield Hills, MI (United States)

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