FDA Inspection 557506 — Datamax Corporation
The FDA completed an inspection of Datamax Corporation on Jan 22, 2009 in Orlando, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 22, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Orlando, FL (United States)