# FDA Inspection 838693 - Wortham Laboratories Inc - July 01, 2013

Source: https://www.keypedia.com/records/fda_inspections/wortham-laboratories-inc/b90d5e43-7d72-497f-9534-e3edfa3fa5df
Source feed: FDA_Inspections

> FDA Inspection 838693 for Wortham Laboratories Inc on July 01, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 838693
- Company Name: Wortham Laboratories Inc
- Inspection Date: 2013-07-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 838693 - 2013-07-01](https://www.keypedia.com/records/fda_inspections/wortham-laboratories-inc/0b1d45e5-d0f4-45dd-bc77-ef009d39c6a5)
- [FDA Inspection 572146 - 2009-03-19](https://www.keypedia.com/records/fda_inspections/wortham-laboratories-inc/a7147a40-0c5c-4bbe-99d1-e56e19216112)

Company: https://www.keypedia.com/companies/wortham-laboratories-inc/df76fd79-b2be-4c27-aa2b-49cb81ab38d7

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