FDA Inspection 1021270 — Becton, Dickinson And Company
The FDA completed an inspection of Becton, Dickinson And Company on May 18, 2017 in Broken Bow, NE. 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
- May 18, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Broken Bow, NE (United States)