# FDA Inspection 1010179 - Techlab, Inc. - April 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/techlab-inc/e69cd88b-b9a2-448e-9615-11e8a27eb334
Source feed: FDA_Inspections

> FDA Inspection 1010179 for Techlab, Inc. on April 26, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010179
- Company Name: Techlab, Inc.
- Inspection Date: 2017-04-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 877648 - 2014-04-14](https://www.keypedia.com/records/fda_inspections/techlab-inc/40020b8d-864e-4dc3-9a86-f658866c037b)
- [FDA Inspection 654252 - 2010-03-25](https://www.keypedia.com/records/fda_inspections/techlab-inc/1a4d5f25-7460-4fc8-859f-374bce04b124)
- [FDA Inspection 654252 - 2010-03-25](https://www.keypedia.com/records/fda_inspections/techlab-inc/37778758-5cf5-491f-afbc-5ad541288316)

Company: https://www.keypedia.com/companies/techlab-inc/7b7a0c11-3859-4809-9044-749e261ea06f

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