# FDA Inspection 630185 - Parker Hannifin/O-Ring - October 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/parker-hannifino-ring/09c746ae-dbf1-4c2f-9fc2-3f2f5c6c5373
Source feed: FDA_Inspections

> FDA Inspection 630185 for Parker Hannifin/O-Ring on October 28, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 630185
- Company Name: Parker Hannifin/O-Ring
- Inspection Date: 2009-10-28
- Classification: No Action Indicated (NAI)
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/parker-hannifino-ring/1afe21f7-9e81-4ed8-b706-b61636ac45c4

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