FDA Inspection
ARCH Medical Solutions - Olive BranchFDA Inspection 1227778 - ARCH Medical Solutions - Olive Branch - January 12, 2024
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Record Details
This FDA Inspection record concerns ARCH Medical Solutions - Olive Branch, with an inspection on January 12, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b862a4a1-38f0-41e8-baeb-d17361eb6a9b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1227778
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of ARCH Medical Solutions - Olive Branch
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 25, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |