FDA Inspection 848893 — Interojo Inc.
The FDA completed an inspection of Interojo Inc. on Jul 18, 2013 in Pyeongtaek City. 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
- Jul 18, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Pyeongtaek City (Korea (the Republic of))