FDA Inspection 592207 — Lofton Label, Inc.
The FDA completed an inspection of Lofton Label, Inc. on Jun 18, 2009 in Inver Grove Heights, MN. 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 18, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Inver Grove Heights, MN (United States)