FDA Inspection
MaxiFlex, LLCMaxiFlex, LLC – FDA Inspection, Dec 20, 2018
Record Details
This FDA Inspection record concerns MaxiFlex, LLC, with an inspection on December 20, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b98fe668-b518-4493-9ea3-6023f480a652
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1075109
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Complaints
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Other FDA inspections of MaxiFlex, LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 11, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MaxiFlex, LLC
- FDA Inspection 734724 - 2011-05-11
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