FDA Inspection
Kayline IncKayline Inc – FDA Inspection, Dec 8, 2011
Record Details
This FDA Inspection record concerns Kayline Inc, with an inspection on December 8, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kayline Inc
- Inspection Date
- December 8, 2011
- Product Type
- Devices
View Company Profile
ID · 92e168ba-702a-4cc4-b1e2-50e20967f163
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 756827
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
- 21 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
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Other FDA inspections of Kayline Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 5, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kayline Inc
- FDA Inspection 650133 - 2010-03-05
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