FDA Inspection
R.K. Manufacturing Corp of ConnecticutR.K. Manufacturing Corp of Connecticut – FDA Inspection, May 4, 2012
Record Details
This FDA Inspection record concerns R.K. Manufacturing Corp of Connecticut, with an inspection on May 4, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- May 4, 2012
- Product Type
- Devices
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ID · 61dae969-c679-4baa-8463-1af510e574e4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 780710
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.75(b)(2)Documentation of validated process performance
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Other FDA inspections of R.K. Manufacturing Corp of Connecticut
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 26, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 6, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 17, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for R.K. Manufacturing Corp of Connecticut
- FDA Inspection 1243937 - 2024-06-26
- FDA Inspection 1065514 - 2018-09-06
- FDA Inspection 905910 - 2014-10-17
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