# Anecare, LLC – FDA Inspection, Mar 2, 2018

Source: https://www.keypedia.com/records/fda_inspections/anecare-llc/dcb28479-058e-4703-b2ab-e524ff8fa8ce
Source feed: FDA_Inspections

> FDA inspection 1045451 of Anecare, LLC, March 02, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1045451
- Company Name: Anecare, LLC
- Inspection Date: 2018-03-02
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.keypedia.com/companies/anecare-llc/8701f944-96ca-4fd2-a6dd-dd34734cf450

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