# Gb Implantat Technologie – FDA Inspection, Aug 16, 2018

Source: https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/32664ba0-bfa8-4a5e-814b-ca9a58aeda5c
Source feed: FDA_Inspections

> FDA inspection 1071168 of Gb Implantat Technologie, August 16, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1071168
- Company Name: Gb Implantat Technologie
- Inspection Date: 2018-08-16
- 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: 0

## Related Documents

- [FDA Inspection 1279033 - 2025-08-21](https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/abde9c48-4597-4804-9b1b-dbc39211cffd)
- FDA Inspection 914433 - 2015-02-11

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

Company: https://www.keypedia.com/companies/gb-implantat-technologie/b0b19567-8554-4140-9626-b87d39b80f26

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