FDA Inspection
First Source IncFirst Source Inc – FDA Inspection, May 25, 2018
Record Details
This FDA Inspection record concerns First Source Inc, with an inspection on May 25, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 7cf18ac5-881f-422e-beb4-d088f51fd855
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1053905
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of First Source Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 24, 2026 | NAI | New York District Office | Postmarket Assurance: Devices |
| September 19, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 20, 2021 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 10, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for First Source Inc
- FDA Inspection 1323488 - 2026-06-24
- FDA Inspection 1218835 - 2023-09-19
- FDA Inspection 1146675 - 2021-07-20
- FDA Inspection 987330 - 2016-06-10
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