# RNK Products, Inc – FDA Inspection, Dec 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/rnk-products-inc/8e2856df-1e72-45b4-b0c4-4d12022f493a
Source feed: FDA_Inspections

> FDA inspection 1038933 of RNK Products, Inc, December 14, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038933
- Company Name: RNK Products, Inc
- Inspection Date: 2017-12-14
- 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: 0

## Related Documents

- [FDA Inspection 926848 - 2015-05-20](https://www.keypedia.com/records/fda_inspections/rnk-products-inc/f73a65ad-741e-41fc-9d87-2cdc9698ae34)
- [FDA Inspection 769356 - 2012-02-23](https://www.keypedia.com/records/fda_inspections/rnk-products-inc/22a9be4b-2def-4e38-8a91-41d2bc694181)
- FDA Inspection 583442 - 2009-05-19

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/rnk-products-inc/14fa20de-c60b-4a83-99bc-91c2c80c820e

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