# Groman Inc. – FDA Inspection, Mar 5, 2018

Source: https://www.keypedia.com/records/fda_inspections/groman-inc/a4b08735-c542-4724-b470-29cbafbff8f5
Source feed: FDA_Inspections

> FDA inspection 1043954 of Groman Inc., March 05, 2018. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1043954
- Company Name: Groman Inc.
- Inspection Date: 2018-03-05
- 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: 3

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- [FDA Inspection 933478 - 2015-07-10](https://www.keypedia.com/records/fda_inspections/groman-inc/72c902c6-df43-44d8-bbb2-d61ae0033c41)
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## Related Officers

- [Company Rep](https://www.keypedia.com/people/stanley-b-eugene/4708f43e-0592-4c24-b276-d9f9092788a3)

Company: https://www.keypedia.com/companies/groman-inc/686baf1e-cba4-484e-ba0b-aa48c492589c

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