FDA Inspection 1117464 — Hillrom Manufacturing, Inc.
The FDA completed an inspection of Hillrom Manufacturing, Inc. on Jan 29, 2020 in Saint Paul, 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
- Jan 29, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Saint Paul, MN (United States)