# Deringer-Ney, Inc. – FDA Inspection, Apr 12, 2019

Source: https://www.keypedia.com/records/fda_inspections/deringer-ney-inc/c0a358bc-93e7-4595-83d3-8d20697d2c1a
Source feed: FDA_Inspections

> FDA inspection 1086270 of Deringer-Ney, Inc., April 12, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1086270
- Company Name: Deringer-Ney, Inc.
- Inspection Date: 2019-04-12
- 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

## Related Documents

- [FDA Inspection 871476 - 2014-02-12](https://www.keypedia.com/records/fda_inspections/deringer-ney-inc/98ad9154-4fd4-44ff-9715-25f73ee30b3b)
- FDA Inspection 734145 - 2011-07-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/eric-c-schmitt/f2716c8c-f06e-4519-a1e7-63a3ef6e07fb)

Company: https://www.keypedia.com/companies/deringer-ney-inc/c3275e91-90d2-4dee-8c8a-6453d9ff6df7

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