# FDA Inspection 1279033 - Gb Implantat Technologie - August 21, 2025

Source: https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/a6da50a4-6e67-43c7-9381-704429e7d54f
Source feed: FDA_Inspections

> FDA Inspection 1279033 for Gb Implantat Technologie on August 21, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279033
- Company Name: Gb Implantat Technologie
- Inspection Date: 2025-08-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## 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 1071168 - 2018-08-16](https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/32664ba0-bfa8-4a5e-814b-ca9a58aeda5c)
- [FDA Inspection 914433 - 2015-02-11](https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/09ec4f50-48e8-4070-ba30-dad38e8e3d4a)

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