# R.K. Manufacturing Corp of Connecticut – FDA Inspection, May 4, 2012

Source: https://www.keypedia.com/records/fda_inspections/rk-manufacturing-corp-of-connecticut/61dae969-c679-4baa-8463-1af510e574e4
Source feed: FDA_Inspections

> FDA inspection 780710 of R.K. Manufacturing Corp of Connecticut, May 04, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 780710
- Company Name: R.K. Manufacturing Corp of Connecticut
- Inspection Date: 2012-05-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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- [FDA Inspection 1065514 - 2018-09-06](https://www.keypedia.com/records/fda_inspections/rk-manufacturing-corp-of-connecticut/9730b229-386b-42ab-bd76-9f7eae307594)
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Company: https://www.keypedia.com/companies/rk-manufacturing-corp-of-connecticut/3b9ef020-79d3-44c3-936f-1615e9466d44

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7