# Sechrist Industries Inc – FDA Inspection, Mar 26, 2010

Source: https://www.keypedia.com/records/fda_inspections/sechrist-industries-inc/eeeaceae-0bec-456a-86cb-3b768639a87d
Source feed: FDA_Inspections

> FDA inspection 654826 of Sechrist Industries Inc, March 26, 2010. Classification: Voluntary Action Indicated (VAI). 14 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 654826
- Company Name: Sechrist Industries Inc
- Inspection Date: 2010-03-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 14

## Related Documents

- FDA Inspection 1181236 - 2022-09-14
- [FDA Inspection 1035020 - 2017-12-15](https://www.keypedia.com/records/fda_inspections/sechrist-industries-inc/5678e47d-6955-471a-a159-9a44197d0493)
- [FDA Inspection 895597 - 2014-09-12](https://www.keypedia.com/records/fda_inspections/sechrist-industries-inc/ccc74d70-acc5-4a46-88fb-bf2ffb92658c)

Company: https://www.keypedia.com/companies/sechrist-industries-inc/1630cdae-6128-45d7-aba5-52211310a438

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