# Cenova AB – FDA Inspection, May 8, 2025

Source: https://www.keypedia.com/records/fda_inspections/cenova-ab/c89966f5-1e57-4482-a861-1e2590c71365
Source feed: FDA_Inspections

> FDA inspection 1269851 of Cenova AB, May 08, 2025. Classification: Voluntary Action Indicated (VAI). 4 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: 1269851
- Company Name: Cenova AB
- Inspection Date: 2025-05-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 4

## Related Documents

- FDA Inspection 1194250 - 2022-11-18
- FDA Inspection 1090521 - 2019-04-12

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/cenova-ab/d4ee8c27-2f15-46f7-9265-d7a5afacc0f4

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