# Aplicare Products, LLC – FDA Inspection, Sep 2, 2016

Source: https://www.keypedia.com/records/fda_inspections/aplicare-products-llc/d9644777-87f8-4955-b1a0-7b45cc269cde
Source feed: FDA_Inspections

> FDA inspection 988787 of Aplicare Products, LLC, September 02, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 211 and 820. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988787
- Company Name: Aplicare Products, LLC
- Inspection Date: 2016-09-02
- 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: 3

## Related Documents

- FDA Inspection 1204284 - 2023-04-14
- [FDA Inspection 1147759 - 2021-08-03](https://www.keypedia.com/records/fda_inspections/aplicare-products-llc/278d4b43-1def-4684-b179-134882dc929e)
- [FDA Inspection 957238 - 2016-01-15](https://www.keypedia.com/records/fda_inspections/aplicare-products-llc/a950abf1-430e-4337-b6b9-635bd184c3fd)
- FDA Inspection 903219 - 2014-11-17
- FDA Inspection 876204 - 2014-04-18

Company: https://www.keypedia.com/companies/aplicare-products-llc/d0c80cfa-4f21-4273-885b-e47212a31fc4

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