FDA Inspection 788350 — WomanCare Global

WomanCare Global — FEI 3008007615

The FDA completed an inspection of WomanCare Global on Jun 15, 2012 in Salem, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 15, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Salem, VA (United States)

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