FDA Inspection
Sechrist Industries IncSechrist Industries Inc – FDA Inspection, Sep 12, 2014
Record Details
This FDA Inspection record concerns Sechrist Industries Inc, with an inspection on September 12, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Sechrist Industries Inc
- Inspection Date
- September 12, 2014
- Product Type
- Devices
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ID · ccc74d70-acc5-4a46-88fb-bf2ffb92658c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 895597
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
- 21 CFR 820.200(b)Analyzing service report
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Other FDA inspections of Sechrist Industries Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 14, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 15, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 26, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Sechrist Industries Inc
- FDA Inspection 1181236 - 2022-09-14
- FDA Inspection 1035020 - 2017-12-15
- FDA Inspection 654826 - 2010-03-26
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