# CFP Acquisitions Inc., Tulsa, OK – FDA Inspections

Source: https://www.keypedia.com/companies/cfp-acquisitions-inc/27cf9a06-4a99-40fd-adff-e6ca4e741871

> Inspection records and compliance data for CFP Acquisitions Inc. in Tulsa, Oklahoma. 3 FDA inspections on record (2 OAI), 1 Form 483, last inspected January 18, 2022.

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## Details

- Name: CFP Acquisitions Inc.
- FEI Number: 3001576820
- Facility Type: Producer of sterile drug products
- Address Line 1: 6136 E 51st St
- City: Tulsa
- State: Oklahoma
- Zip Code: 74135
- Country Name: United States
- Address: 6136 E 51st St, Tulsa, Oklahoma 74135, United States
- Country: United States

## Related Documents

- [483 - CFP Acquisitions Inc. - 2022-12-08](https://www.keypedia.com/records/483/cfp-acquisitions-inc/87a6f235-4b88-4552-8fbb-f095a670cff7) — source: FDA, date: December 8, 2022
- [483 - CFP Acquisitions Inc. - 2022-01-18](https://www.keypedia.com/records/483/cfp-acquisitions-inc/6a3f1c7d-2931-494b-a015-f1affe552bab) — source: FDA, date: January 18, 2022
- [FDA Inspection 1161167 - CFP Acquisitions Inc. - 2022-01-18](https://www.keypedia.com/records/fda_inspections/cfp-acquisitions-inc/986dba68-3cfb-450f-8bb3-9d8ed192e56f) — classification: Official Action Indicated (OAI), source: FDA, date: January 18, 2022
- [483 - CFP Acquisitions Inc. - 2018-07-11](https://www.keypedia.com/records/483/cfp-acquisitions-inc/550f74b4-6e44-4882-af4a-0d4a5076336f) — source: FDA, date: July 11, 2018
- [FDA Inspection 1058647 - CFP Acquisitions Inc. - 2018-07-11](https://www.keypedia.com/records/fda_inspections/cfp-acquisitions-inc/205c686d-09c8-4ecf-b2b4-c7249057d72e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 11, 2018
- [483 - CFP Acquisitions Inc. - 2015-07-23](https://www.keypedia.com/records/483/cfp-acquisitions-inc/9ef9d19e-4bd1-4e34-8497-c08f562bba4a) — source: FDA, date: July 23, 2015
- [FDA Inspection 917724 - CFP Acquisitions Inc. - 2015-03-13](https://www.keypedia.com/records/fda_inspections/cfp-acquisitions-inc/c05258db-e9f7-4cc4-9819-7400b5cfcf21) — classification: Official Action Indicated (OAI), source: FDA, date: March 13, 2015

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