FDA Inspection 1082633 — Honeywell Safety Products USA, Inc.
The FDA completed an inspection of Honeywell Safety Products USA, Inc. on Dec 10, 2018 in San Diego, CA. 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 10, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- San Diego, CA (United States)