# RLC Labs Inc. - Inspection Records

Source: https://www.keypedia.com/companies/rlc-labs-inc/1b81a5c1-d6cf-4440-8359-bc59f096d8db

> Inspection records and compliance data for RLC Labs Inc. in Phoenix, Arizona. Access full analysis and detailed observations.

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## Details

- Name: RLC Labs Inc.
- FEI Number: 3002523846
- City: Phoenix
- State: Arizona
- Country Name: United States
- Address Line 1: 1850 E Riverview Dr
- Zip Code: 85034

## Related Documents

- [483 - RLC Labs Inc. - 2023-11-02](https://www.keypedia.com/records/483/rlc-labs-inc/177c1f22-e20c-4bc1-8b53-7a77a3bf1193) — source: FDA, date: November 2, 2023
- [FDA Inspection 1221698 - RLC Labs Inc. - 2023-11-02](https://www.keypedia.com/records/fda_inspections/rlc-labs-inc/6faef532-a668-4623-aafd-6a78800a9ce3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 2, 2023
- [483 - RLC Labs Inc. - 2023-09-15](https://www.keypedia.com/records/483/rlc-labs-inc/13248e54-e3eb-4a32-a851-5714545af81e) — source: FDA, date: September 15, 2023
- [483 - RLC Labs Inc. - 2021-11-04](https://www.keypedia.com/records/483/rlc-labs-inc/acb9c71f-7da5-4202-9afd-14df307a7ff1) — source: FDA, date: November 4, 2021
- [FDA Inspection 1156014 - RLC Labs Inc. - 2021-11-04](https://www.keypedia.com/records/fda_inspections/rlc-labs-inc/e4065663-c9d1-402c-ae02-4931abfb003d) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2021
- [FDA Inspection 1156014 - RLC Labs Inc. - 2021-11-04](https://www.keypedia.com/records/fda_inspections/rlc-labs-inc/4d00ad40-3656-4df3-9c91-05a2374be55a) — classification: Official Action Indicated (OAI), source: FDA, date: November 4, 2021
- [483 - RLC Labs Inc. - 2020-03-05](https://www.keypedia.com/records/483/rlc-labs-inc/b0600bfd-f720-4bf2-a5bf-07bf9a1b95ba) — source: FDA, date: March 5, 2020
- [WARNING_LETTER - RLC Labs Inc. - 2020-03-05](https://www.keypedia.com/records/warning_letter/rlc-labs-inc/c3c5b827-dca9-406d-b2d3-6ba1340c15e9) — source: FDA, date: March 5, 2020
- [FDA Inspection 1021606 - RLC Labs Inc. - 2017-08-11](https://www.keypedia.com/records/fda_inspections/rlc-labs-inc/e1f21871-5f53-46c0-9ea7-94918777af74) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2017
- [FDA Inspection 766950 - RLC Labs Inc. - 2012-02-08](https://www.keypedia.com/records/fda_inspections/rlc-labs-inc/4d1b30f0-953f-47fd-8956-4ac61cb2fdba) — classification: No Action Indicated (NAI), source: FDA, date: February 8, 2012
- [FDA Inspection 703127 - RLC Labs Inc. - 2010-12-15](https://www.keypedia.com/records/fda_inspections/rlc-labs-inc/9a98cfd4-ff2e-482a-bef8-3d3b2b50c18d) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2010
- [FDA Inspection 564408 - RLC Labs Inc. - 2009-01-26](https://www.keypedia.com/records/fda_inspections/rlc-labs-inc/55193239-60cb-4df6-aa8b-7aa62449a252) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2009

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- [Program Division Director](https://www.keypedia.com/people/steven-e-porter/5448db0e-32f0-4e98-8a5f-9f0857373b06)
