FDA Inspection 663170 — Mediplast Israel Ltd.
The FDA completed an inspection of Mediplast Israel Ltd. on May 2, 2010 in Yavne. 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
- May 2, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Yavne (Israel)