FDA Inspection 1038765 — An Viet Manufacturing
The FDA completed an inspection of An Viet Manufacturing on December 6, 2017 in Binh Duong. 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
- December 6, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Binh Duong (Vietnam)