FDA Inspection
Eprt Technologies Inc Dba ThrisointEprt Technologies Inc Dba Thrisoint – FDA Inspection, Apr 20, 2012
Record Details
This FDA Inspection record concerns Eprt Technologies Inc Dba Thrisoint, with an inspection on April 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- April 20, 2012
- Product Type
- Devices
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ID · b3c65b0b-7093-49c0-b2bb-25d3670cc362
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 783154
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(b)Review and evaluation for investigation
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Other FDA inspections of Eprt Technologies Inc Dba Thrisoint
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 9, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Eprt Technologies Inc Dba Thrisoint
- FDA Inspection 941351 - 2015-09-09
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