# FDA Inspection 982018 - Acme Monaco Corporation - August 24, 2016

Source: https://www.keypedia.com/records/fda_inspections/acme-monaco-corporation/9bcdbfc3-8771-47cf-a2f5-54b11e2d5abc
Source feed: FDA_Inspections

> FDA Inspection 982018 for Acme Monaco Corporation on August 24, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982018
- Company Name: Acme Monaco Corporation
- Inspection Date: 2016-08-24
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/acme-monaco-corporation/703a1e2b-88fb-4175-8191-76f39b69bdc3

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