# FDA Inspection 850702 - STERIMED, Inc. - September 27, 2013

Source: https://www.keypedia.com/records/fda_inspections/sterimed-inc/edc68029-ed69-4637-8a3b-c2933fc07b4d
Source feed: FDA_Inspections

> FDA Inspection 850702 for STERIMED, Inc. on September 27, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 850702
- Company Name: STERIMED, Inc.
- Inspection Date: 2013-09-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/sterimed-inc/699ab6a1-3094-4076-97f1-799cc072234c

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