FDA Inspection
Becton Dickinson & Co.Becton Dickinson & Co. – FDA Inspection, Aug 4, 2017
Record Details
This FDA Inspection record concerns Becton Dickinson & Co., with an inspection on August 4, 2017, issued by the Baltimore District Office, covering medical devices & rad health.
View Company Profile
ID · 4087cbda-19d0-458b-bc67-d7fa565cd6b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1020632
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Becton Dickinson & Co.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| August 1, 2025 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 11, 2025 | Not classified | Baltimore District Office | Compliance: Medical Devices |
| July 23, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 26, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| May 11, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Becton Dickinson & Co.
- FDA Inspection 1268801 - 2025-08-01
- FDA Inspection 1264435 - 2025-04-11
- FDA Inspection 1147022 - 2021-07-23
- FDA Inspection 1001333 - 2017-01-26
- FDA Inspection 926020 - 2015-05-11
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.