# FDA Inspection 925054 - Arjo (Suzhou) Co., Ltd. - April 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/arjo-suzhou-co-ltd/817d8026-d05c-4f8a-8049-faf27c5aa119
Source feed: FDA_Inspections

> FDA Inspection 925054 for Arjo (Suzhou) Co., Ltd. on April 23, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 925054
- Company Name: Arjo (Suzhou) Co., Ltd.
- Inspection Date: 2015-04-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 756296 - 2011-11-24](https://www.keypedia.com/records/fda_inspections/arjo-suzhou-co-ltd/e5e21106-a9f6-4059-a50a-814478512c77)

Company: https://www.keypedia.com/companies/arjo-suzhou-co-ltd/10206bd5-a5d5-4cf2-8eaa-23335ad3e989

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