# K.C. Pharmaceuticals, Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/kc-pharmaceuticals-inc/c82c2f64-5944-429b-a3a9-2f7a567e47d3

> Inspection records and compliance data for K.C. Pharmaceuticals, Inc in Pomona, California. Access full analysis and detailed observations.

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## Details

- Name: K.C. Pharmaceuticals, Inc
- FEI Number: 2026940
- City: Pomona
- State: California
- Country Name: United States
- Address Line 1: 3215 Producer Way
- Zip Code: 91768

## Related Documents

- [FDA Inspection 1294070 - K.C. Pharmaceuticals, Inc - 2026-02-13](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/cd0d8819-eb97-4026-b57a-60b8938692d8) — source: FDA, date: February 13, 2026
- [483 - K.C. Pharmaceuticals, Inc - 2024-08-28](https://www.globalkeysolutions.net/records/483/kc-pharmaceuticals-inc/42bdb612-a9ab-4ece-b326-86e0cd897a7c) — source: FDA, date: August 28, 2024
- [FDA Inspection 1247201 - K.C. Pharmaceuticals, Inc - 2024-08-28](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/4d2997fd-981a-47b9-b559-199031f88ad1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 28, 2024
- [483 - K.C. Pharmaceuticals, Inc - 2023-02-13](https://www.globalkeysolutions.net/records/483/kc-pharmaceuticals-inc/7f927619-2f9a-494b-bf17-5943a9949adf) — source: FDA, date: February 13, 2023
- [FDA Inspection 1197242 - K.C. Pharmaceuticals, Inc - 2023-02-13](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/f2890018-3936-4ea6-93ba-08683d11590a) — classification: Official Action Indicated (OAI), source: FDA, date: February 13, 2023
- [483 - K.C. Pharmaceuticals, Inc - 2020-01-30](https://www.globalkeysolutions.net/records/483/kc-pharmaceuticals-inc/62f4d6c3-b675-4e9c-b5a4-08a1a7831a2a) — source: FDA, date: January 30, 2020
- [FDA Inspection 1116341 - K.C. Pharmaceuticals, Inc - 2020-01-30](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/78f9da67-71fe-4721-bde3-5e1eb4ee0ad5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 30, 2020
- [483 - K.C. Pharmaceuticals, Inc - 2017-11-16](https://www.globalkeysolutions.net/records/483/kc-pharmaceuticals-inc/13310105-63c4-44ce-8bd9-876aae4d9f4f) — source: FDA, date: November 16, 2017
- [FDA Inspection 1032267 - K.C. Pharmaceuticals, Inc - 2017-11-16](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/643dc654-deba-47c6-ac43-ac4a9c15f43b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2017
- [FDA Inspection 923526 - K.C. Pharmaceuticals, Inc - 2015-03-19](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/34828028-1a8a-42e2-9f01-fdeecede8a1c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 19, 2015
- [FDA Inspection 881454 - K.C. Pharmaceuticals, Inc - 2014-05-23](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/f7392984-8ced-4f34-a4c5-1249bce4f6e1) — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2014
- [FDA Inspection 881454 - K.C. Pharmaceuticals, Inc - 2014-05-23](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/a27eb59e-125b-4520-bbd1-85a7297b5ac4) — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2014
- [FDA Inspection 881454 - K.C. Pharmaceuticals, Inc - 2014-05-23](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/5a3e07f8-b522-43e5-8802-91a749bc223e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2014
- [FDA Inspection 835302 - K.C. Pharmaceuticals, Inc - 2013-06-10](https://www.globalkeysolutions.net/records/fda_inspections/kc-pharmaceuticals-inc/bc48589c-a1c5-48bc-b24b-89ae349c4de1) — classification: No Action Indicated (NAI), source: FDA, date: June 10, 2013
- [483 - K.C. Pharmaceuticals, Inc - 2009-12-30](https://www.globalkeysolutions.net/records/483/kc-pharmaceuticals-inc/cf0f74a9-6c8b-4e64-a901-284bbf398402) — source: FDA, date: December 30, 2009

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