FDA Inspection 1075139 — Fresenius Kabi USA LLC
The FDA completed an inspection of Fresenius Kabi USA LLC on Dec 3, 2018 in Melrose Park, 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
- Dec 3, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Melrose Park, IL (United States)