# Steripac – FDA Inspection, Jul 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/steripac/4fe9b308-bcc5-4fbb-89f1-97e1c5f3aaa7
Source feed: FDA_Inspections

> FDA inspection 602130 of Steripac, July 30, 2009. Classification: Official Action Indicated (OAI). 11 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 602130
- Company Name: Steripac
- Inspection Date: 2009-07-30
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 11

## Related Documents

- FDA Inspection 717982 - 2011-04-06

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