# FDA Inspection 897767 - Intermetro Industries Corp. - September 29, 2014

Source: https://www.keypedia.com/records/fda_inspections/intermetro-industries-corp/94495c99-1d14-47a0-8798-8d8e15d973f4
Source feed: FDA_Inspections

> FDA Inspection 897767 for Intermetro Industries Corp. on September 29, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897767
- Company Name: Intermetro Industries Corp.
- Inspection Date: 2014-09-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/intermetro-industries-corp/bf656f8f-d6d4-488e-a5e4-3b2298d8b3d7

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