# EUROMI S.A. – FDA Inspection, Jan 15, 2015

Source: https://www.keypedia.com/records/fda_inspections/euromi-sa/a1269fe5-8d65-44ff-ba72-77c67c0559e4
Source feed: FDA_Inspections

> FDA inspection 914498 of EUROMI S.A., January 15, 2015. Classification: Official Action Indicated (OAI). 14 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 914498
- Company Name: EUROMI S.A.
- Inspection Date: 2015-01-15
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 14

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Company: https://www.keypedia.com/companies/euromi-sa/117d63e2-e079-4816-8804-517c2fde2bf6

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