FDA Inspection 785785 — Cylex, Inc.
The FDA completed an inspection of Cylex, Inc. on Jun 11, 2012 in Columbia, MD. 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
- Jun 11, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Columbia, MD (United States)