# FDA Inspection 717982 - Steripac - April 06, 2011

Source: https://www.keypedia.com/records/fda_inspections/steripac/d7bc79f5-eff8-435f-9ffe-4216c0b24a3d
Source feed: FDA_Inspections

> FDA Inspection 717982 for Steripac on April 06, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 717982
- Company Name: Steripac
- Inspection Date: 2011-04-06
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 717982 - 2011-04-06](https://www.keypedia.com/records/fda_inspections/steripac/ee413633-5df7-407f-84a7-08139c372722)
- [FDA Inspection 602130 - 2009-07-30](https://www.keypedia.com/records/fda_inspections/steripac/2b22c745-664d-471f-9980-aeda453826a7)
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Company: https://www.keypedia.com/companies/steripac/58ac33a0-9aef-411c-aeda-83cf484ca149

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