FDA Inspection 894029 — Playtex Manufacturing Inc.

Playtex Manufacturing Inc. — FEI 2515444

The FDA completed an inspection of Playtex Manufacturing Inc. on Sep 4, 2014 in Dover, DE. 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
Sep 4, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Dover, DE (United States)

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