FDA Inspection 726576 — 4 Everyoung

4 Everyoung — FEI 3006394053

The FDA completed an inspection of 4 Everyoung on May 27, 2011 in Memphis, TN. 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
May 27, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)

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