# Lingraphicare America, Inc. – FDA Inspection, Aug 4, 2022

Source: https://www.keypedia.com/records/fda_inspections/lingraphicare-america-inc/90752a9d-7a12-4264-bf1f-d38d45b7fd6b
Source feed: FDA_Inspections

> FDA inspection 1177262 of Lingraphicare America, Inc., August 04, 2022. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1177262
- Company Name: Lingraphicare America, Inc.
- Inspection Date: 2022-08-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1261187 - 2025-02-03](https://www.keypedia.com/records/fda_inspections/lingraphicare-america-inc/bfb10226-9c1d-4dd0-b23d-bf3d1a8463bb)
- FDA Inspection 1109991 - 2019-11-15
- [FDA Inspection 1002305 - 2017-02-15](https://www.keypedia.com/records/fda_inspections/lingraphicare-america-inc/c0c4ea2f-122a-4fa2-8c7e-69e0f779a11e)
- FDA Inspection 883463 - 2014-06-24
- FDA Inspection 759639 - 2011-12-21

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