FDA Inspection 659539 — Claritec Company
The FDA completed an inspection of Claritec Company on Apr 26, 2010 in Round Lake, IL. 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
- Apr 26, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Round Lake, IL (United States)