MANA PRODUCTS, INC.
FDA inspection history in Long Island City, New York, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Long Island City, New York.
Cited most
Across all MANA PRODUCTS observations on file
- 21 CFR 211.160(b)(4)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete MANA PRODUCTS file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Long Island City, New York
One Form 483 · 2022 · 3 observations
Latest: Form 483, Oct 17, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-10-17 | 483 Form 483 | Long Island City, New York | 3 | $99 |
Investigators on these documents
FEI number 2430738 · most recent document Oct 17, 2022
About MANA PRODUCTS, INC.
How many FDA Form 483s has MANA PRODUCTS, INC. received?
FDA Intel has 1 Form 483 on file for MANA PRODUCTS, INC.; the most recent is dated Oct 17, 2022.
When was MANA PRODUCTS, INC. last inspected by FDA?
The most recent FDA inspection document on file for MANA PRODUCTS, INC. is a Form 483 dated Oct 17, 2022, for the site in Long Island City, New York.
What did FDA cite at MANA PRODUCTS, INC.?
The regulations cited most in the observations on file for MANA PRODUCTS, INC. are 21 CFR 211.160(b)(4) (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.