FDA Inspection 640881 — Digital Lightwave, Inc.
The FDA completed an inspection of Digital Lightwave, Inc. on Jan 27, 2010 in Clearwater, 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 27, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Clearwater, FL (United States)