FDA Inspection 991799 — Teva Womens Health, LLC

Teva Womens Health, LLC — FEI 1526814

The FDA completed an inspection of Teva Womens Health, LLC on Nov 10, 2016 in Cincinnati, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 10, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Cincinnati, OH (United States)

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