# Groman Inc. – FDA Inspection, Mar 7, 2023

Source: https://www.keypedia.com/records/fda_inspections/groman-inc/f70689dd-24db-4901-b864-a88d4b9b73c0
Source feed: FDA_Inspections

> FDA inspection 1206335 of Groman Inc., March 07, 2023. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1206335
- Company Name: Groman Inc.
- Inspection Date: 2023-03-07
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1308980 - 2026-03-17
- [FDA Inspection 1043954 - 2018-03-05](https://www.keypedia.com/records/fda_inspections/groman-inc/a4b08735-c542-4724-b470-29cbafbff8f5)
- [FDA Inspection 933478 - 2015-07-10](https://www.keypedia.com/records/fda_inspections/groman-inc/72c902c6-df43-44d8-bbb2-d61ae0033c41)
- FDA Inspection 700357 - 2010-12-03

## Related Officers

- [Dianiris C. Ayala](https://www.keypedia.com/people/dianiris-c-ayala/ba6c5538-201b-4c9a-8f23-e160db6868e6)

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