FDA Inspection
ARCH Medical Solutions - MemphisARCH Medical Solutions - Memphis – FDA Inspection, Feb 7, 2014
Record Details
This FDA Inspection record concerns ARCH Medical Solutions - Memphis, with an inspection on February 7, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 7, 2014
- Product Type
- Devices
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ID · ed6d7856-9fbf-4729-b2f8-09d942359d4b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 865030
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.22Quality audits - auditor independence
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of ARCH Medical Solutions - Memphis
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 7, 2026 | Not classified | New Orleans District Office | |
| July 8, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 3, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for ARCH Medical Solutions - Memphis
- FDA Inspection 1318312 - 2026-05-07
- FDA Inspection 1175523 - 2022-07-08
- FDA Inspection 1031428 - 2017-08-03
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