# Oberg Medical Products Company – FDA Inspection, Mar 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/oberg-medical-products-company/5da2c245-5d11-412f-83d5-90e5a0a9f060
Source feed: FDA_Inspections

> FDA inspection 1082715 of Oberg Medical Products Company, March 15, 2019. Classification: No Action Indicated (NAI). 5 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1082715
- Company Name: Oberg Medical Products Company
- Inspection Date: 2019-03-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1224078 - 2023-11-15
- FDA Inspection 1016277 - 2017-04-06

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/katelyn-a-staub-zamperini/bb7f95a4-53c1-473c-856e-517312bdba30)

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