# FDA Inspection 839340 - Vitalograph (Ireland), Ltd. - May 23, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/vitalograph-ireland-ltd/fb29e501-31e6-4f0f-bd68-aee958a3826f
Source feed: FDA_Inspections

> FDA Inspection 839340 for Vitalograph (Ireland), Ltd. on May 23, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 839340
- Company Name: Vitalograph (Ireland), Ltd.
- Inspection Date: 2013-05-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 839340 - 2013-05-23](https://www.globalkeysolutions.net/records/fda_inspections/vitalograph-ireland-ltd/6f3bdc32-5d8b-4c40-a41e-9597798b9b99)
- [FDA Inspection 750637 - 2011-09-15](https://www.globalkeysolutions.net/records/fda_inspections/vitalograph-ireland-ltd/a1dab9c3-789c-440d-8725-f0384357f0fd)
- [FDA Inspection 750637 - 2011-09-15](https://www.globalkeysolutions.net/records/fda_inspections/vitalograph-ireland-ltd/8177be4d-964b-40f6-a0ce-c1adea895a7e)

Company: https://www.globalkeysolutions.net/companies/vitalograph-ireland-ltd/a12a744d-2f8b-43aa-b6ce-8069e4a9cc99

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