FDA Inspection 660391 — Cytophil, Inc.
The FDA completed an inspection of Cytophil, Inc. on May 6, 2010 in East Troy, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- May 6, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- East Troy, WI (United States)