# OSCILLA A/S – FDA Inspection, Sep 1, 2026

Source: https://www.keypedia.com/records/fda_inspections/oscilla-as/56ae09eb-e315-4439-beff-908a5a7dea4e
Source feed: FDA_Inspections

> FDA inspection 1333720 of OSCILLA A/S, September 01, 2026. Classification: No Action Indicated (NAI). 1 citation. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1333720
- Company Name: OSCILLA A/S
- Inspection Date: 2026-09-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/eric-c-schmitt/f2716c8c-f06e-4519-a1e7-63a3ef6e07fb)

Company: https://www.keypedia.com/companies/oscilla-as/b1f2d100-5e64-47ae-8a3d-f7867d5f4b81

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8