# Microfit, Inc. – FDA Inspection, Aug 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/microfit-inc/d5763744-3647-484f-9931-1e7fb92973cc
Source feed: FDA_Inspections

> FDA inspection 1063445 of Microfit, Inc., August 20, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063445
- Company Name: Microfit, Inc.
- Inspection Date: 2018-08-20
- 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: 2

## Related Documents

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- FDA Inspection 927254 - 2015-05-27
- [FDA Inspection 752333 - 2011-11-09](https://www.keypedia.com/records/fda_inspections/microfit-inc/40f6d680-f79f-4450-9582-cf61743a3201)

## Related Officers

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

Company: https://www.keypedia.com/companies/microfit-inc/45db7b86-b047-447a-b14f-4d2c599ce2f9

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