# FDA Inspection 914433 - Gb Implantat Technologie - February 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/09ec4f50-48e8-4070-ba30-dad38e8e3d4a
Source feed: FDA_Inspections

> FDA Inspection 914433 for Gb Implantat Technologie on February 11, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 914433
- Company Name: Gb Implantat Technologie
- Inspection Date: 2015-02-11
- Classification: No Action Indicated (NAI)
- 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 1279033 - 2025-08-21](https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/a6da50a4-6e67-43c7-9381-704429e7d54f)
- [FDA Inspection 1071168 - 2018-08-16](https://www.keypedia.com/records/fda_inspections/gb-implantat-technologie/32664ba0-bfa8-4a5e-814b-ca9a58aeda5c)

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