# de Gotzen S.r.l. – FDA Inspection, Dec 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/de-gotzen-srl/994697ee-7fbe-4ed4-b306-9199c0504550
Source feed: FDA_Inspections

> FDA inspection 1037479 of de Gotzen S.r.l., December 21, 2017. Classification: Official Action Indicated (OAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037479
- Company Name: de Gotzen S.r.l.
- Inspection Date: 2017-12-21
- 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: 0

## Related Officers

- [Investigator](https://www.keypedia.com/people/ashley-a-mutawakkil/512be391-fd96-451c-9569-98e43cfba9db)

Company: https://www.keypedia.com/companies/de-gotzen-srl/ae22dfbc-dde3-48d7-8af9-f221a235cd66

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