# BALT USA, LLC – FDA Inspection, Jul 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/balt-usa-llc/f56994fb-9ff1-4f02-9dba-153e6e756596
Source feed: FDA_Inspections

> FDA inspection 1210642 of BALT USA, LLC, July 21, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210642
- Company Name: BALT USA, LLC
- Inspection Date: 2023-07-21
- 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: 6

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- FDA Inspection 1120825 - 2020-03-12
- FDA Inspection 958563 - 2016-02-18
- FDA Inspection 793968 - 2012-05-22

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/marlo-ian-m-alintanahin/a37da927-b369-4753-b275-41743556f25e)

Company: https://www.keypedia.com/companies/balt-usa-llc/6783eb4f-96f7-4c7c-80d9-4447fdb185cc

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