FDA Inspection
Nypro, Inc.Nypro, Inc. – FDA Inspection, Jul 6, 2016
Record Details
This FDA Inspection record concerns Nypro, Inc., with an inspection on July 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Nypro, Inc.
- Inspection Date
- July 6, 2016
- Product Type
- Devices
View Company Profile
ID · 78dba60e-f6d8-4ec8-8902-c825fa8d4ea1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 984364
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Nypro, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 22, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 27, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Nypro, Inc.
- FDA Inspection 1242404 - 2024-05-22
- FDA Inspection 1059960 - 2018-06-27
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