FDA Inspection 1041617 — LISI MEDICAL Remmele, Inc.
The FDA completed an inspection of LISI MEDICAL Remmele, Inc. on January 26, 2018 in Coon Rapids, MN. 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
- January 26, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Coon Rapids, MN (United States)