# FDA Inspection 1068252 - Cellpack Ag - September 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/cellpack-ag/7700d605-59ec-484d-b968-638e8b77afa6
Source feed: FDA_Inspections

> FDA Inspection 1068252 for Cellpack Ag on September 20, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1068252
- Company Name: Cellpack Ag
- Inspection Date: 2018-09-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1312090 - 2026-02-12](https://www.globalkeysolutions.net/records/fda_inspections/cellpack-ag/d2d7ec5b-1a15-47a0-8d8c-03ca25bc9eaa)
- [FDA Inspection 881940 - 2014-05-01](https://www.globalkeysolutions.net/records/fda_inspections/cellpack-ag/1219f5e7-b9a6-4c34-9b09-37eadaf6d902)

Company: https://www.globalkeysolutions.net/companies/cellpack-ag/bf51fd44-3732-49eb-ac20-eb17e9f49a2c

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