FDA Inspection
Neomedix CorporationNeomedix Corporation – FDA Inspection, Dec 29, 2011
Record Details
This FDA Inspection record concerns Neomedix Corporation, with an inspection on December 29, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neomedix Corporation
- Inspection Date
- December 29, 2011
- Product Type
- Devices
View Company Profile
ID · 74102939-e837-40dd-8f06-305e85a4cf2b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 761781
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.25(b)Training records
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Neomedix Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 19, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 29, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 19, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Neomedix Corporation
- FDA Inspection 1098182 - 2019-06-19
- FDA Inspection 1047029 - 2018-03-29
- FDA Inspection 896544 - 2014-09-19
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