FDA Inspection
Casco Manufacturing Solutions IncCasco Manufacturing Solutions Inc – FDA Inspection, Jun 2, 2017
Record Details
This FDA Inspection record concerns Casco Manufacturing Solutions Inc, with an inspection on June 2, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Teresa K. Kastner
View Company Profile
ID · fe97274e-2fe0-49c2-99ba-8070ece58ca0
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1012543
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.40Procedures not adequately established or maintained
- 21 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
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Other FDA inspections of Casco Manufacturing Solutions Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 14, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 10, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Casco Manufacturing Solutions Inc
- FDA Inspection 1109809 - 2019-11-14
- FDA Inspection 781424 - 2012-05-10
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