FDA Inspection 572516 — Lexamed, Ltd
The FDA completed an inspection of Lexamed, Ltd on Mar 13, 2009 in Toledo, OH. 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
- Mar 13, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Toledo, OH (United States)
Additional Details
Postmarket Audit Inspections