FDA Inspection
Stericycle IncStericycle Inc – FDA Inspection, Dec 21, 2023
Record Details
This FDA Inspection record concerns Stericycle Inc, with an inspection on December 21, 2023, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · b15a3ccb-0034-4b55-ab67-a9ad94f8fda6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1226105
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Stericycle Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 21, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Stericycle Inc
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.