FDA Inspection
Nypro Inc.Nypro Inc. – FDA Inspection, Feb 23, 2018
Record Details
This FDA Inspection record concerns Nypro Inc., with an inspection on February 23, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c6f93d36-bbba-4c67-8de1-597519e4dcde
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1041994
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.184DHR content
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Nypro Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| September 17, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 2, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 12, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 9, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Nypro Inc.
- FDA Inspection 1284728 - 2025-09-17
- FDA Inspection 916197 - 2015-03-02
- FDA Inspection 798297 - 2012-09-12
- FDA Inspection 613007 - 2009-09-09
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