Caraco Pharmaceutical Laboratories
FDA inspection history in Farmington Hills, Michigan, 2008
- 1
- EIR
- 1
- Form 483
Every document, by year
- EIR
- Form 483
2008: one inspection report and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2008One inspection report and one Form 483, at Farmington Hills, Michigan.
Cited most
Across all Caraco Pharmaceutical Laboratories observations on file
- 21 CFR 211.182Equipment cleaning and use log2
- 21 CFR 211.130Packaging and labeling operations1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Caraco Pharmaceutical Laboratories file.
All 2 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
Farmington Hills, Michigan
One inspection report and one Form 483 · 2008 · 5 observations
Latest: EIR, Dec 22, 2008 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2008-12-22 | EIR EIR | Farmington Hills, Michigan | — | $550 |
| 2008-12-22 | 483 Form 483 | Farmington Hills, Michigan | 5 | $99 |
Investigators on these documents
Adam J. Wilson (2)Jonathan R. Loving (2)Patsy J. Domingo (2)
FEI number 3006389940 · most recent document Dec 22, 2008
About Caraco Pharmaceutical Laboratories
How many FDA Form 483s has Caraco Pharmaceutical Laboratories received?
FDA Intel has 1 Form 483 on file for Caraco Pharmaceutical Laboratories; the most recent is dated Dec 22, 2008.
When was Caraco Pharmaceutical Laboratories last inspected by FDA?
The most recent FDA inspection document on file for Caraco Pharmaceutical Laboratories is an establishment inspection report (EIR) dated Dec 22, 2008, for the site in Farmington Hills, Michigan.
What did FDA cite at Caraco Pharmaceutical Laboratories?
The regulations cited most in the observations on file for Caraco Pharmaceutical Laboratories are 21 CFR 211.182 (Equipment cleaning and use log), 2 times; 21 CFR 211.130 (Packaging and labeling operations), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.