# Lingraphicare America, Inc. – FDA Inspection, Feb 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/lingraphicare-america-inc/c0c4ea2f-122a-4fa2-8c7e-69e0f779a11e
Source feed: FDA_Inspections

> FDA inspection 1002305 of Lingraphicare America, Inc., February 15, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002305
- Company Name: Lingraphicare America, Inc.
- Inspection Date: 2017-02-15
- 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: 4

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- [FDA Inspection 1261187 - 2025-02-03](https://www.keypedia.com/records/fda_inspections/lingraphicare-america-inc/bfb10226-9c1d-4dd0-b23d-bf3d1a8463bb)
- [FDA Inspection 1177262 - 2022-08-04](https://www.keypedia.com/records/fda_inspections/lingraphicare-america-inc/90752a9d-7a12-4264-bf1f-d38d45b7fd6b)
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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/loretta-nemchik/37791f6d-862a-4863-9295-1cca43f9fe3a)

Company: https://www.keypedia.com/companies/lingraphicare-america-inc/4f47f1e2-0d44-4ffa-8f31-79fdb892b071

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