Turbare Manufacturing
FDA inspection history in Conway, Arkansas, 2025 to 2026
- 2
- Form 483s
- 1
- Warning letter
Every document, by year
- Form 483
- Warning letter
2025: one warning letter and one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025–26Two Form 483s and one warning letter, at Conway, Arkansas.
- 2025The longest 483 on file: 8 observations over 7 pages at Conway, Arkansas.
Cited most
Across all Turbare Manufacturing observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.192Production record review2
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.165(d)Testing and release for distribution1
The complete Turbare Manufacturing file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Conway, Arkansas
Two Form 483s and one warning letter · 2025 to 2026 · 12 observations
Latest: Form 483, May 7, 2026 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-05-07 | 483 Form 483 | Conway, Arkansas | 4 | $99 |
| 2025-09-16 | Warning letter Warning letter | Conway, Arkansas | — | $99 |
| 2025-01-24 | 483 Form 483 | Conway, Arkansas | 8 | $99 |
Investigators on these documents
FEI number 3027507354 · most recent document May 7, 2026
About Turbare Manufacturing
How many FDA Form 483s has Turbare Manufacturing received?
FDA Intel has 2 Form 483s on file for Turbare Manufacturing; the most recent is dated May 7, 2026.
When was Turbare Manufacturing last inspected by FDA?
The most recent FDA inspection document on file for Turbare Manufacturing is a Form 483 dated May 7, 2026, for the site in Conway, Arkansas.
What did FDA cite at Turbare Manufacturing?
The regulations cited most in the observations on file for Turbare Manufacturing are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.100(a) (Written procedures; deviations), 1 time.
Has Turbare Manufacturing received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Turbare Manufacturing; the most recent is dated Sep 16, 2025.