FDA Inspection
Oberg Medical Products CompanyOberg Medical Products Company – FDA Inspection, Mar 15, 2019
Record Details
This FDA Inspection record concerns Oberg Medical Products Company, with an inspection on March 15, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 5da2c245-5d11-412f-83d5-90e5a0a9f060
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1082715
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Complaints
- 21 CFR 820.75(a)Documentation
- 21 CFR 820.90(a)Nonconforming product control
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Oberg Medical Products Company
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 15, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 6, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Oberg Medical Products Company
- FDA Inspection 1224078 - 2023-11-15
- FDA Inspection 1016277 - 2017-04-06
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