# EUROMI S.A. – FDA Inspection, Apr 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/euromi-sa/ba62fcc8-1806-4dbf-9e65-d034c50fe7a1
Source feed: FDA_Inspections

> FDA inspection 1016083 of EUROMI S.A., April 21, 2017. 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016083
- Company Name: EUROMI S.A.
- Inspection Date: 2017-04-21
- 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: 6

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

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

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