FDA Inspection
Medicomp, Inc. dba ReactDXMedicomp, Inc. dba ReactDX – FDA Inspection, Aug 11, 2011
Record Details
This FDA Inspection record concerns Medicomp, Inc. dba ReactDX, with an inspection on August 11, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medicomp, Inc. dba ReactDX
- Inspection Date
- August 11, 2011
- Product Type
- Devices
View Company Profile
ID · 75ddd5bd-4bec-4404-9a16-1a42a297bc10
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 739532
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.198(e)Records of complaint investigation
- 21 CFR 820.30(g)Design validation - Risk analysis
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medicomp, Inc. dba ReactDX
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 30, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 20, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 16, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medicomp, Inc. dba ReactDX
- FDA Inspection 1217172 - 2023-08-30
- FDA Inspection 1029758 - 2017-10-20
- FDA Inspection 887569 - 2014-07-16
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