# ARMM Inc – FDA Inspection, Feb 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/armm-inc/c3b086aa-79af-4bdf-b217-b8f8b11e3773
Source feed: FDA_Inspections

> FDA inspection 1041014 of ARMM Inc, February 12, 2018. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1041014
- Company Name: ARMM Inc
- Inspection Date: 2018-02-12
- 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: 7

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- [FDA Inspection 1087440 - 2019-04-16](https://www.keypedia.com/records/fda_inspections/armm-inc/f66fcf21-cd05-48ca-ab0e-702a2cac6e8d)
- FDA Inspection 912585 - 2015-02-04
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## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kirtida-patel/c62852cf-9724-4296-bc4b-de8993dcf716)

Company: https://www.keypedia.com/companies/armm-inc/78815c8e-a19c-4e1b-9e21-626871a9b25b

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