# Q LABS, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/q-labs-llc/3923e3f2-bd54-4e3a-b482-901a7807f845

> Inspection records and compliance data for Q LABS, LLC in Cincinnati, Ohio. Access full analysis and detailed observations.

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## Details

- Name: Q LABS, LLC
- FEI Number: 1527260
- City: Cincinnati
- State: Ohio
- Country Name: United States
- Address Line 1: 1930 Radcliff Dr
- Zip Code: 45204
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [483 - Q LABS, LLC - 2025-04-25](https://www.globalkeysolutions.net/records/483/q-labs-llc/a25ebc6b-7909-4103-a334-6ac58a49ef1e) — source: FDA, date: April 25, 2025
- [FDA Inspection 1268075 - Q LABS, LLC - 2025-04-25](https://www.globalkeysolutions.net/records/fda_inspections/q-labs-llc/5149e134-f0d9-40b9-8c00-45626e0833f2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 25, 2025
- [483 - Q LABS, LLC - 2019-11-21](https://www.globalkeysolutions.net/records/483/q-labs-llc/67684f99-327b-463c-aec6-0aeb06518093) — source: FDA, date: November 21, 2019
- [FDA Inspection 1110791 - Q LABS, LLC - 2019-11-21](https://www.globalkeysolutions.net/records/fda_inspections/q-labs-llc/66580f30-e741-4eda-ae33-c26d2f0203ac) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 21, 2019
- [FDA Inspection 993084 - Q LABS, LLC - 2016-11-18](https://www.globalkeysolutions.net/records/fda_inspections/q-labs-llc/b0185481-3d12-47ca-9db8-bdf851b0f007) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2016
- [FDA Inspection 786335 - Q LABS, LLC - 2012-05-31](https://www.globalkeysolutions.net/records/fda_inspections/q-labs-llc/7a200664-df34-4288-b400-b1abdf3e57a4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 31, 2012
- [FDA Inspection 665933 - Q LABS, LLC - 2010-06-10](https://www.globalkeysolutions.net/records/fda_inspections/q-labs-llc/ac3e1609-7fa2-4cf7-9bb7-f998960ca351) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 10, 2010

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