FDA Inspection
NUCMEDCOR (NH), LLCNUCMEDCOR (NH), LLC – FDA Inspection, Aug 7, 2015
Record Details
This FDA Inspection record concerns NUCMEDCOR (NH), LLC, with an inspection on August 7, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- NUCMEDCOR (NH), LLC
- Inspection Date
- August 7, 2015
- Product Type
- Devices
View Company Profile
ID · e9b80a84-83b2-4e72-b724-75bbd73d9417
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 940286
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(b)(1)Documentation of disposition, justification, signature
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Other FDA inspections of NUCMEDCOR (NH), LLC
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 27, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 21, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 11, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for NUCMEDCOR (NH), LLC
- FDA Inspection 1081747 - 2019-02-27
- FDA Inspection 832368 - 2013-05-21
- FDA Inspection 723996 - 2011-05-11
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