FDA Inspection 831555 — Hiossen Inc.
The FDA completed an inspection of Hiossen Inc. on Apr 18, 2013 in Fairless Hills, PA. 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
- Apr 18, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Fairless Hills, PA (United States)