FDA Inspection
Medline Industries - Arlington HeightsMedline Industries - Arlington Heights – FDA Inspection, May 12, 2010
Record Details
This FDA Inspection record concerns Medline Industries - Arlington Heights, with an inspection on May 12, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- May 12, 2010
- Product Type
- Devices
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ID · 02f43b29-e18c-4e07-8cb7-838cbc45f363
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 666778
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(a)(1)Analysis of data sources
- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.184(b)Quantity manufactured
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Other FDA inspections of Medline Industries - Arlington Heights
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2026 | Not classified | Chicago District Office | Compliance: Medical Devices |
| December 6, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 17, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 28, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 24, 2013 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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