FDA Inspection
ClearLine MDClearLine MD – FDA Inspection, Oct 29, 2014
Record Details
This FDA Inspection record concerns ClearLine MD, with an inspection on October 29, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- ClearLine MD
- Inspection Date
- October 29, 2014
- Product Type
- Devices
View Company Profile
ID · 9c14675a-616f-46e8-9af6-4132ee4294ca
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 901658
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.75(a)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of ClearLine MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 8, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for ClearLine MD
- FDA Inspection 1042336 - 2018-02-08
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