Turbare Manufacturing
Form 483 issued May 7, 2026 · Conway, Arkansas
- Inspection
- Apr 20 – May 7, 2026
- Investigator
- Sangeeta M. Khurana
- Observations
- 4
- Pages
- 13
- FEI number
- 3027507354
In short: On May 7, 2026, FDA issued a Form 483 with 4 observations to Turbare Manufacturing in Conway, Arkansas (FEI 3027507354) after an inspection that ran Apr 20 – May 7, 2026. The investigator was Sangeeta M. Khurana. Most observations concern quality system and production.
At a glance
Quality system and production account for 4 of 4 observations.
What FDA observed
Preview: the opening words of each observationDashed: section inferred by FDA Intel and checked against the regulation text
- 01
The responsibilities and procedures applicable to the quality control unit…
- 02
Procedures designed to prevent microbiological contamination of drug products purporting to be…
- 03
Production personnel were not practicing good…
- 04
There is a failure to thoroughly review any unexplained discrepancy and the failure of a batch…
This inspection in context
Sangeeta M. Khurana
20 documents · 2014–2026
Cites 211.113 (control of microbiological contamination) more than any other section. Most of their documents are for sites in California.
The firmTurbare Manufacturing history
All 3 documents on file for this site, in date order, with what was cited at each inspection.
Similar 483sOther sites cited under 211.22
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Turbare Manufacturing?
FDA listed 4 observations on this Form 483, mostly about quality system and production. The opening words of each observation are shown on this page.
Who inspected Turbare Manufacturing?
Sangeeta M. Khurana is named on this Form 483, for the inspection of Apr 20 – May 7, 2026. Each investigator has a profile showing what they cite most.
When was Turbare Manufacturing inspected by FDA?
The inspection ran Apr 20 – May 7, 2026, and the Form 483 is dated May 7, 2026.
How do I get the full Form 483 for Turbare Manufacturing?
Download the original PDF from FDA Intel for $99, with no subscription. Your first Form 483 or letter is on us. You also get an invoice PDF with the order.