# Apneicare LLC dba Patient Safety Inc. – FDA Inspection, Aug 23, 2022

Source: https://www.keypedia.com/records/fda_inspections/apneicare-llc-dba-patient-safety-inc/6cef26bb-eaf6-4b60-a471-8b8147285254
Source feed: FDA_Inspections

> FDA inspection 1178056 of Apneicare LLC dba Patient Safety Inc., August 23, 2022. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1178056
- Company Name: Apneicare LLC dba Patient Safety Inc.
- Inspection Date: 2022-08-23
- 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 1236625 - 2024-04-12](https://www.keypedia.com/records/fda_inspections/apneicare-llc-dba-patient-safety-inc/c4a406ca-e888-4d54-aec2-6d0363c22ab0)
- [FDA Inspection 1019443 - 2017-07-26](https://www.keypedia.com/records/fda_inspections/apneicare-llc-dba-patient-safety-inc/caed01d1-0f6a-4094-ae60-e6ef7d87ef17)
- [FDA Inspection 924046 - 2015-05-05](https://www.keypedia.com/records/fda_inspections/apneicare-llc-dba-patient-safety-inc/39b3a75a-2165-4ecf-bdaa-9d15cf2539b6)
- FDA Inspection 710837 - 2011-02-18

Company: https://www.keypedia.com/companies/apneicare-llc-dba-patient-safety-inc/dcf788e6-0728-42cc-b0ae-59b5ddc51343

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