# Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy - Inspection Records

Source: https://www.globalkeysolutions.net/companies/anderson-compounding-pharmacy-inc-dba-anderson-compounding-pharmacy/20b196d7-a331-4ad7-a833-cf8a1674d55e

> Inspection records and compliance data for Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy in Bristol, Tennessee. Access full analysis and detailed observations.

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## Details

- Name: Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy
- FEI Number: 3014877770
- City: Bristol
- State: Tennessee
- Country Name: United States
- Address Line 1: 310 Bluff City Hwy
- Zip Code: 37620
- Facility Type: Producer of Sterile and Non-Sterile Human and Veterinarian Drugs

## Related Documents

- [FDA Inspection 1153267 - Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy - 2021-09-09](https://www.globalkeysolutions.net/records/fda_inspections/anderson-compounding-pharmacy-inc-dba-anderson-compounding-pharmacy/95b91f3a-019b-4dca-a7d6-0863a8576cf4) — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2021
- [WARNING_LETTER - Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy - 2019-04-05](https://www.globalkeysolutions.net/records/warning_letter/anderson-compounding-pharmacy-inc-dba-anderson-compounding-pharmacy/43aad766-cc4b-43a3-91aa-9db8c67ff34d) — source: FDA, date: April 5, 2019
- [483 - Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy - 2019-04-05](https://www.globalkeysolutions.net/records/483/anderson-compounding-pharmacy-inc-dba-anderson-compounding-pharmacy/3cc1ddc7-fba4-4b4b-9955-2991f7929011) — source: FDA, date: April 5, 2019
- [FDA Inspection 1085801 - Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy - 2019-04-05](https://www.globalkeysolutions.net/records/fda_inspections/anderson-compounding-pharmacy-inc-dba-anderson-compounding-pharmacy/75f49936-c24b-4474-ba32-16d5855e1045) — classification: Official Action Indicated (OAI), source: FDA, date: April 5, 2019

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