FDA Inspection 991799 — Teva Womens Health, LLC

Teva Womens Health, LLC — FEI 1526814

The FDA completed an inspection of Teva Womens Health, LLC on November 10, 2016 in Cincinnati, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

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