# Groman Inc. – FDA Inspection, Jul 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/groman-inc/72c902c6-df43-44d8-bbb2-d61ae0033c41
Source feed: FDA_Inspections

> FDA inspection 933478 of Groman Inc., July 10, 2015. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 933478
- Company Name: Groman Inc.
- Inspection Date: 2015-07-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

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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