FDA Inspection 1037310 — Hansol Medical
The FDA completed an inspection of Hansol Medical on Nov 9, 2017 in Paju-si. 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 9, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Paju-si (Korea (the Republic of))