FDA Inspection 1171697 — Hillrom Manufacturing, Inc.
The FDA completed an inspection of Hillrom Manufacturing, Inc. on Apr 26, 2022 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
- Apr 26, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Saint Paul, MN (United States)