FDA Inspection 1116630 — Aea Srl
The FDA completed an inspection of Aea Srl on January 10, 2020 in Maiolati Spontini. 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
- January 10, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Maiolati Spontini (Italy)