FDA Inspection
Nasiff Associates, IncNasiff Associates, Inc – FDA Inspection, Nov 16, 2015
Record Details
This FDA Inspection record concerns Nasiff Associates, Inc, with an inspection on November 16, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Nasiff Associates, Inc
- Inspection Date
- November 16, 2015
- Product Type
- Devices
View Company Profile
ID · 03ad743c-ed00-46e5-9236-9efa88bc1765
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 950978
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.80(e)Documentation
- 21 CFR 820.198(a)Complaints
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Nasiff Associates, Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 11, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 29, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Nasiff Associates, Inc
- FDA Inspection 1117498 - 2020-02-11
- FDA Inspection 805317 - 2012-10-29
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