FDA Inspection
Ranir, LLCRanir, LLC – FDA Inspection, Aug 16, 2017
Record Details
This FDA Inspection record concerns Ranir, LLC, with an inspection on August 16, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Cynthia L. Aycock (Issuing Officer)
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ID · 47ff44a1-a591-4ed1-bd08-cd460c4e4dfe
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1021914
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Ranir, LLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 28, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 27, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Ranir, LLC
- FDA Inspection 951697 - 2015-10-28
- FDA Inspection 866413 - 2014-02-27
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