FDA Inspection
Ludlow Technical Products Canada Ltd(A Division of Cardinal Health)Ludlow Technical Products Canada Ltd(A Division of Cardinal Health) – FDA Inspection, Jan 28, 2016
Record Details
This FDA Inspection record concerns Ludlow Technical Products Canada Ltd(A Division of Cardinal Health), with an inspection on January 28, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 28, 2016
- Product Type
- Devices
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ID · ae647e38-c98a-409e-8093-3e7551cf868f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 961724
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
- 21 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures
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Other FDA inspections of Ludlow Technical Products Canada Ltd(A Division of Cardinal Health)
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 12, 2023 | NAI | Bioresearch Monitoring | |
| March 21, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Ludlow Technical Products Canada Ltd(A Division of Cardinal Health)
- FDA Inspection 1198500 - 2023-01-12
- FDA Inspection 823780 - 2013-03-21
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