# FDA Inspection 1197616 - DimcoGray Inc. - February 09, 2023

Source: https://www.keypedia.com/records/fda_inspections/dimcogray-inc/879716bb-df8e-405d-80fe-d17ea24de585
Source feed: FDA_Inspections

> FDA Inspection 1197616 for DimcoGray Inc. on February 09, 2023. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1197616
- Company Name: DimcoGray Inc.
- Inspection Date: 2023-02-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1096699 - 2019-06-28](https://www.keypedia.com/records/fda_inspections/dimcogray-inc/9727f8d9-9eaf-4f2a-b7e2-c2aa92135691)
- [FDA Inspection 1066895 - 2018-09-17](https://www.keypedia.com/records/fda_inspections/dimcogray-inc/8f50a694-1c71-41e1-b22c-6d51597b5544)
- [FDA Inspection 1008218 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/dimcogray-inc/3e27f4f0-c714-4b18-8202-f3d563d962cd)
- [FDA Inspection 1008218 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/dimcogray-inc/b3ce0a0a-7097-4ade-a665-fe3808cd3783)
- [FDA Inspection 865402 - 2014-02-07](https://www.keypedia.com/records/fda_inspections/dimcogray-inc/4d9f1e84-c2e7-46de-9d29-507b6ae219d0)

Company: https://www.keypedia.com/companies/dimcogray-inc/9ea4c42d-f2c7-429f-aad2-3259ae7e1d00

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