# M.R.S. SRL – FDA Inspection, Jan 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/mrs-srl/f71cb057-373a-4f67-ae02-229b59ef6132
Source feed: FDA_Inspections

> FDA inspection 1007202 of M.R.S. SRL, January 26, 2017. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007202
- Company Name: M.R.S. SRL
- Inspection Date: 2017-01-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1262424 - 2025-01-16

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/mrs-srl/5a6afc34-8c79-49a2-9a9f-da00a9cc5e79

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