FDA Inspection
MEDLINE RENEWALMEDLINE RENEWAL – FDA Inspection, Aug 3, 2010
Record Details
This FDA Inspection record concerns MEDLINE RENEWAL, with an inspection on August 3, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- MEDLINE RENEWAL
- Inspection Date
- August 3, 2010
- Product Type
- Devices
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ID · 9d26adcf-85f1-4945-9448-6db6d40d911e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 674222
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(b)Documentation
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Other FDA inspections of MEDLINE RENEWAL
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 2, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MEDLINE RENEWAL
- FDA Inspection 590921 - 2009-06-02
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