FDA Inspection
David R. Liljenquist, M.D.David R. Liljenquist, M.D. – FDA Inspection, Oct 30, 2009
Record Details
This FDA Inspection record concerns David R. Liljenquist, M.D., with an inspection on October 30, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- David R. Liljenquist, M.D.
- Inspection Date
- October 30, 2009
- Product Type
- Devices
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ID · 47f6c303-31ba-4141-b78e-ce1a16a88745
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 630237
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of David R. Liljenquist, M.D.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 5, 2024 | Not classified | Seattle District Office | |
| August 3, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| April 17, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for David R. Liljenquist, M.D.
- FDA Inspection 1235497 - 2024-04-05
- FDA Inspection 1065396 - 2018-08-03
- FDA Inspection 924149 - 2015-04-17
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