# FDA Inspection 863242 - Vetter Pharma Fertigung GmbH & Co. KG - December 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/vetter-pharma-fertigung-gmbh-co-kg/a29a64fc-2b7f-4a0f-ab35-7a5c0d5f996f
Source feed: FDA_Inspections

> FDA Inspection 863242 for Vetter Pharma Fertigung GmbH & Co. KG on December 05, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 863242
- Company Name: Vetter Pharma Fertigung GmbH & Co. KG
- Inspection Date: 2013-12-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1248795 - 2024-09-20](https://www.keypedia.com/records/fda_inspections/vetter-pharma-fertigung-gmbh-co-kg/1c303c5b-09c0-49eb-a402-b5c1add5218e)
- [FDA Inspection 1241531 - 2022-07-13](https://www.keypedia.com/records/fda_inspections/vetter-pharma-fertigung-gmbh-co-kg/352159f5-97ea-485d-8014-44ac3ab27489)
- [FDA Inspection 1129698 - 2019-09-11](https://www.keypedia.com/records/fda_inspections/vetter-pharma-fertigung-gmbh-co-kg/f4e720bf-d094-4b37-aad0-f432670d9a94)
- [FDA Inspection 1000875 - 2017-01-17](https://www.keypedia.com/records/fda_inspections/vetter-pharma-fertigung-gmbh-co-kg/b558ef9e-1f16-4247-802d-bdc447e850e3)
- [FDA Inspection 931820 - 2015-01-20](https://www.keypedia.com/records/fda_inspections/vetter-pharma-fertigung-gmbh-co-kg/fc0b10da-15ea-4dc2-b429-f93b712d215b)

Company: https://www.keypedia.com/companies/vetter-pharma-fertigung-gmbh-co-kg/6b51041e-37a7-4672-a7e2-c3c871d6231b

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