# FDA Inspection 1073332 - Indilab, Inc. - November 28, 2018

Source: https://www.keypedia.com/records/fda_inspections/indilab-inc/acfaaea2-c85e-4af3-bfea-92ddcdbab2bd
Source feed: FDA_Inspections

> FDA Inspection 1073332 for Indilab, Inc. on November 28, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073332
- Company Name: Indilab, Inc.
- Inspection Date: 2018-11-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/indilab-inc/f9eaad19-45e3-4ded-a668-1baa2bebbc52

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