FDA Inspection 1114841 — IVF Michigan

IVF Michigan — FEI 3010929692

The FDA completed an inspection of IVF Michigan on Dec 4, 2019 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
Dec 4, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bloomfield Hills, MI (United States)

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