# FDA Inspection 1224078 - Oberg Medical Products Company - November 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/oberg-medical-products-company/0d31ec8c-3512-4bde-8d54-e50121e9e985
Source feed: FDA_Inspections

> FDA Inspection 1224078 for Oberg Medical Products Company on November 15, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1224078
- Company Name: Oberg Medical Products Company
- Inspection Date: 2023-11-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1224078 - 2023-11-15](https://www.keypedia.com/records/fda_inspections/oberg-medical-products-company/a3b2da43-d609-40f3-95bd-5e6f53023280)
- [FDA Inspection 1082715 - 2019-03-15](https://www.keypedia.com/records/fda_inspections/oberg-medical-products-company/39c4db6f-f1a0-4a03-a2bf-52acec83a1e2)
- [FDA Inspection 1082715 - 2019-03-15](https://www.keypedia.com/records/fda_inspections/oberg-medical-products-company/5da2c245-5d11-412f-83d5-90e5a0a9f060)
- [FDA Inspection 1016277 - 2017-04-06](https://www.keypedia.com/records/fda_inspections/oberg-medical-products-company/5484f1b5-fbb6-4810-b4cf-b17f78792e42)

Company: https://www.keypedia.com/companies/oberg-medical-products-company/f66fa08a-3e5a-4af3-8854-0107eeacc28e

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7