# FDA Inspection 629476 - NIPRO CORP. - October 29, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/nipro-corp/f98c79c1-97a0-4fe8-8341-0f027029404e/
Source feed: FDA_Inspections

> FDA Inspection 629476 for NIPRO CORP. on October 29, 2009. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 629476
- Company Name: NIPRO CORP.
- Inspection Date: 2009-10-29
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1238561 - 2024-04-24](https://www.globalkeysolutions.net/api/records/fda_inspections/nipro-corp/3297e846-4744-4c99-a09c-47a4ee8ad580/)
- [FDA Inspection 1238561 - 2024-04-24](https://www.globalkeysolutions.net/api/records/fda_inspections/nipro-corp/24c0ce82-5342-43b0-8799-dd6f9b2debc4/)
- [FDA Inspection 1061549 - 2018-07-05](https://www.globalkeysolutions.net/api/records/fda_inspections/nipro-corp/8dfb7b8f-6b31-413e-b61b-666d867ce366/)
- [FDA Inspection 1061549 - 2018-07-05](https://www.globalkeysolutions.net/api/records/fda_inspections/nipro-corp/70b88d10-7a1d-4af8-b3df-5f8413f0c8f9/)
- [FDA Inspection 928639 - 2015-04-16](https://www.globalkeysolutions.net/api/records/fda_inspections/nipro-corp/ced03232-3859-4b1e-8493-f431246b3ea6/)

Company: https://www.globalkeysolutions.net/companies/nipro-corp/5a61a305-4198-40c8-a1fa-a8c07ec96acc

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