# M.D.L. S.r.l. – FDA Inspection, Sep 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/mdl-srl/fcde5677-d520-4058-87ce-7919b95d755b
Source feed: FDA_Inspections

> FDA inspection 1102625 of M.D.L. S.r.l., September 19, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102625
- Company Name: M.D.L. S.r.l.
- Inspection Date: 2019-09-19
- 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: 2

## Related Documents

- [FDA Inspection 1235461 - 2024-02-15](https://www.keypedia.com/records/fda_inspections/mdl-srl/f6be5903-9f14-47ab-aa59-146b3277a287)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)

Company: https://www.keypedia.com/companies/mdl-srl/0290653b-2c56-4c4b-a0de-442bb133a02f

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