# FDA Inspection 843186 - Wexford Labs Inc - August 02, 2013

Source: https://www.keypedia.com/records/fda_inspections/wexford-labs-inc/9b965a82-94eb-44fd-971b-6c6b9591a12d
Source feed: FDA_Inspections

> FDA Inspection 843186 for Wexford Labs Inc on August 02, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 843186
- Company Name: Wexford Labs Inc
- Inspection Date: 2013-08-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 909365 - 2015-01-07](https://www.keypedia.com/records/fda_inspections/wexford-labs-inc/e635b102-1a04-4ddb-8212-7eb693de25dd)
- [FDA Inspection 809406 - 2012-12-06](https://www.keypedia.com/records/fda_inspections/wexford-labs-inc/50a8545f-3730-4669-8a19-5dfe5fbe2d1e)

Company: https://www.keypedia.com/companies/wexford-labs-inc/3245ac18-70eb-4f18-b2db-51ef3ee5dfb0

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