FDA Inspection
SIPVSIPV – FDA Inspection, May 24, 2018
Record Details
This FDA Inspection record concerns SIPV, with an inspection on May 24, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e3a386e0-f55a-43c5-bf8f-612a3533fbb7
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1053051
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.70(a)Production processes
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of SIPV
5| Date | Classification | Office | Project area |
|---|---|---|---|
| March 19, 2026 | Not classified | Office of Inspections and Investigations | |
| March 19, 2026 | Not classified | Office of Inspections and Investigations | |
| October 26, 2023 | Not classified | Office of Inspections and Investigations | |
| June 25, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 24, 2008 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for SIPV
- FDA Inspection 1317210 - 2026-03-19
- FDA Inspection 1316810 - 2026-03-19
- FDA Inspection 1226577 - 2023-10-26
- FDA Inspection 934487 - 2015-06-25
- FDA Inspection 547695 - 2008-10-24
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