# Transcoject GmbH – FDA Inspection, Mar 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/transcoject-gmbh/73c6c8d1-fd3d-4d41-b985-d30e1b51fff4
Source feed: FDA_Inspections

> FDA inspection 1004177 of Transcoject GmbH, March 09, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004177
- Company Name: Transcoject GmbH
- Inspection Date: 2017-03-09
- 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: 1

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- [FDA Inspection 917902 - 2015-02-19](https://www.keypedia.com/records/fda_inspections/transcoject-gmbh/9894c400-a62c-413f-9da4-9c6a037c1672)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/transcoject-gmbh/910de755-7091-4d47-b24b-65c3d9f3fd2d

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