FDA Inspection
Xitron Technologies IncXitron Technologies Inc – FDA Inspection, Jul 10, 2009
Record Details
This FDA Inspection record concerns Xitron Technologies Inc, with an inspection on July 10, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Xitron Technologies Inc
- Inspection Date
- July 10, 2009
- Product Type
- Devices
View Company Profile
ID · 8846688d-4797-4095-957b-6f7907106fff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 593436
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
- 21 CFR 820.40(a)Not approved or obsolete document retrieval
- 21 CFR 820.70(c)Environmental control system periodic inspections
- 21 CFR 820.180(b)Retention period
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